Canonical Allele Identifier: CA50474016
Community Standard Title: NM_004082.5(DCTN1):c.3621C>T (p.Leu1207=)
Gene: DCTN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74362130G>A , CM000664.2:g.74362130G>A GRCh38
NC_000002.11:g.74589257G>A , CM000664.1:g.74589257G>A GRCh37
NC_000002.10:g.74442765G>A NCBI36
NG_008735.2:g.34958C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004082.5:c.3621C>T MANE Select NP_004073.2:p.Leu1207=
ENST00000628224.3:c.3621C>T MANE Select ENSP00000487279.2:p.Leu1207=
NM_001135040.2:c.3546C>T NP_001128512.1:p.Leu1182=
NM_001135040.3:c.3546C>T NP_001128512.1:p.Leu1182=
NM_001135041.2:c.3204C>T NP_001128513.1:p.Leu1068=
NM_001135041.3:c.3204C>T NP_001128513.1:p.Leu1068=
NM_001190836.1:c.3495C>T NP_001177765.1:p.Leu1165=
NM_001190836.2:c.3495C>T NP_001177765.1:p.Leu1165=
NM_001190837.1:c.3600C>T NP_001177766.1:p.Leu1200=
NM_001190837.2:c.3600C>T NP_001177766.1:p.Leu1200=
NM_001378991.1:c.3570C>T NP_001365920.1:p.Leu1190=
NM_001378992.1:c.3552C>T NP_001365921.1:p.Leu1184=
NM_004082.4:c.3621C>T NP_004073.2:p.Leu1207=
NM_023019.3:c.3219C>T NP_075408.1:p.Leu1073=
NM_023019.4:c.3219C>T NP_075408.1:p.Leu1073=
NR_033935.1:n.3890C>T
NR_033935.2:n.3669C>T
ENST00000361874.7:c.3621C>T ENSP00000354791.3:p.Leu1207=
ENST00000361874.8:c.3606C>T ENSP00000354791.4:p.Leu1202=
ENST00000394003.7:c.3600C>T ENSP00000377571.3:p.Leu1200=
ENST00000409240.5:c.3495C>T ENSP00000386406.1:p.Leu1165=
ENST00000409438.5:c.3204C>T ENSP00000387270.1:p.Leu1068=
ENST00000409567.7:c.3546C>T ENSP00000386843.3:p.Leu1182=
ENST00000409868.5:c.3555C>T ENSP00000387327.1:p.Leu1185=
ENST00000434055.5:c.*905C>T ENSP00000416711.1:n.*905C>T
ENST00000451608.2:c.360C>T ENSP00000416453.2:p.Leu120=
ENST00000466110.5:n.4858C>T
ENST00000491465.5:n.1884C>T
ENST00000492717.1:n.292C>T
ENST00000497666.1:n.97-593C>T
ENST00000628224.2:c.3555C>T ENSP00000487279.1:p.Leu1185=
ENST00000633691.1:c.3219C>T ENSP00000487724.1:p.Leu1073=
ENST00000680606.1:c.3570C>T ENSP00000505612.1:p.Leu1190=