Canonical Allele Identifier: CA384358805

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32731480T>A , CM000674.2:g.32731480T>A GRCh38
NC_000012.11:g.32884414T>A , CM000674.1:g.32884414T>A GRCh37
NC_000012.10:g.32775681T>A NCBI36
NG_012219.1:g.57278T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000434676.7:c.*691T>A (DNM1L) ENSP00000390090.2:n.*691T>A
ENST00000546757.6:c.*1011T>A (DNM1L) ENSP00000448105.2:n.*1011T>A
ENST00000547078.6:c.1364T>A (DNM1L) ENSP00000448802.2:p.Ile455Asn
ENST00000547719.2:n.2958T>A (DNM1L)
ENST00000547932.6:c.*691T>A (DNM1L) ENSP00000515272.1:n.*691T>A
ENST00000548671.6:c.*872T>A (DNM1L) ENSP00000515271.1:n.*872T>A
ENST00000548750.6:c.1238T>A (DNM1L) ENSP00000447788.2:p.Ile413Asn
ENST00000549926.6:c.878T>A (DNM1L) ENSP00000515263.1:p.Ile293Asn
ENST00000550011.6:c.*1315T>A (DNM1L) ENSP00000515261.1:n.*1315T>A
ENST00000550093.6:n.1412T>A (DNM1L)
ENST00000551076.6:c.*942T>A (DNM1L) ENSP00000515275.1:n.*942T>A
ENST00000551476.6:c.1274T>A (DNM1L) ENSP00000447845.2:p.Ile425Asn
ENST00000551643.6:c.*1156T>A (DNM1L) ENSP00000450401.1:n.*1156T>A
ENST00000703337.1:c.*1122T>A (DNM1L) ENSP00000515262.1:n.*1122T>A
ENST00000703338.1:c.878T>A (DNM1L) ENSP00000515264.1:p.Ile293Asn
ENST00000703360.1:c.*1011T>A (DNM1L) ENSP00000515270.1:n.*1011T>A
ENST00000703361.1:c.956T>A (DNM1L) ENSP00000515273.1:p.Ile319Asn
ENST00000703362.1:c.*691T>A (DNM1L) ENSP00000515274.1:n.*691T>A
ENST00000703363.1:n.2946T>A (DNM1L)
ENST00000703364.1:n.3023T>A (DNM1L)
ENST00000703365.1:c.*190T>A (DNM1L) ENSP00000515276.1:n.*190T>A
ENST00000703366.1:n.2385T>A (DNM1L)
ENST00000703367.1:c.1325T>A (DNM1L) ENSP00000515277.1:p.Ile442Asn
ENST00000703368.1:c.*872T>A (DNM1L) ENSP00000515278.1:n.*872T>A
ENST00000703369.1:c.956T>A (DNM1L) ENSP00000515279.1:p.Ile319Asn
ENST00000703370.1:c.878T>A (DNM1L) ENSP00000515280.1:p.Ile293Asn
ENST00000703371.1:c.878T>A (DNM1L) ENSP00000515281.1:p.Ile293Asn
ENST00000703372.1:c.1118T>A (DNM1L) ENSP00000515282.1:p.Ile373Asn
ENST00000549701.6:c.1325T>A (DNM1L) MANE Select ENSP00000450399.1:p.Ile442Asn
ENST00000553257.6:c.1364T>A (DNM1L) MANE Plus Clinical ENSP00000449089.1:p.Ile455Asn
ENST00000266481.10:c.1325T>A (DNM1L) ENSP00000266481.6:p.Ile442Asn
ENST00000358214.9:c.1364T>A (DNM1L) ENSP00000350948.5:p.Ile455Asn
ENST00000381000.8:c.1364T>A (DNM1L) ENSP00000370388.4:p.Ile455Asn
ENST00000414834.6:c.716T>A (DNM1L) ENSP00000404160.2:p.Ile239Asn
ENST00000452533.6:c.1325T>A (DNM1L) ENSP00000415131.2:p.Ile442Asn
ENST00000546649.5:c.*567T>A (DNM1L) ENSP00000448936.1:n.*567T>A
ENST00000546757.5:c.1176T>A (DNM1L) ENSP00000448105.1:n.1176T>A
ENST00000547312.5:c.1325T>A (DNM1L) ENSP00000448610.1:p.Ile442Asn
ENST00000549701.5:c.1325T>A (DNM1L) ENSP00000450399.1:p.Ile442Asn
ENST00000550093.5:n.12T>A (DNM1L)
ENST00000551673.5:n.460-3961A>T (YARS2)
ENST00000553257.5:c.1364T>A (DNM1L) ENSP00000449089.1:p.Ile455Asn
NM_001278463.1:c.1325T>A (DNM1L) NP_001265392.1:p.Ile442Asn
NM_001278464.1:c.1364T>A (DNM1L) NP_001265393.1:p.Ile455Asn
NM_001278465.1:c.1364T>A (DNM1L) NP_001265394.1:p.Ile455Asn
NM_001278466.1:c.716T>A (DNM1L) NP_001265395.1:p.Ile239Asn
NM_005690.4:c.1325T>A (DNM1L) NP_005681.2:p.Ile442Asn
NM_012062.4:c.1325T>A (DNM1L) NP_036192.2:p.Ile442Asn
NM_012063.3:c.1325T>A (DNM1L) NP_036193.2:p.Ile442Asn
XM_005253282.3:c.1364T>A (DNM1L) XP_005253339.1:p.Ile455Asn
XM_005253283.3:c.878T>A (DNM1L) XP_005253340.1:p.Ile293Asn
XM_011520543.1:c.1364T>A (DNM1L) XP_011518845.1:p.Ile455Asn
XM_011520544.1:c.668T>A (DNM1L) XP_011518846.1:p.Ile223Asn
XR_242891.3:n.1832+152A>T (YARS2)
XR_242892.3:n.1650-6115A>T (YARS2)
XR_429036.1:n.1707+152A>T (YARS2)
XR_931297.1:n.1832+152A>T (YARS2)
XR_931298.1:n.1707+152A>T (YARS2)
XR_931299.1:n.1650-3961A>T (YARS2)
NM_001330380.1:c.1364T>A (DNM1L) NP_001317309.1:p.Ile455Asn
XM_011520543.3:c.1364T>A (DNM1L) XP_011518845.1:p.Ile455Asn
XM_011520544.2:c.668T>A (DNM1L) XP_011518846.1:p.Ile223Asn
XM_017018663.2:c.668T>A (DNM1L) XP_016874152.1:p.Ile223Asn
XM_017018664.1:c.668T>A (DNM1L) XP_016874153.1:p.Ile223Asn
XM_017018665.1:c.668T>A (DNM1L) XP_016874154.1:p.Ile223Asn
XR_001748730.2:n.2272-6115A>T (YARS2)
XR_002957331.1:n.2147-3961A>T (YARS2)
XR_242892.5:n.2147-6115A>T (YARS2)
NM_012062.5:c.1325T>A (DNM1L) MANE Select NP_036192.2:p.Ile442Asn
NM_001278463.2:c.1325T>A (DNM1L) NP_001265392.1:p.Ile442Asn
NM_001278464.2:c.1364T>A (DNM1L) MANE Plus Clinical NP_001265393.1:p.Ile455Asn
NM_001278465.2:c.1364T>A (DNM1L) NP_001265394.1:p.Ile455Asn
NM_001278466.2:c.716T>A (DNM1L) NP_001265395.1:p.Ile239Asn
NM_001330380.2:c.1364T>A (DNM1L) NP_001317309.1:p.Ile455Asn
NM_005690.5:c.1325T>A (DNM1L) NP_005681.2:p.Ile442Asn
NM_012063.4:c.1325T>A (DNM1L) NP_036193.2:p.Ile442Asn