Canonical Allele Identifier: CA1722254

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74370534G>A , CM000664.2:g.74370534G>A	GRCh38
NC_000002.11:g.74597661G>A , CM000664.1:g.74597661G>A	GRCh37
NC_000002.10:g.74451169G>A	NCBI36
NG_008735.2:g.26554C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004082.5:c.1059C>T MANE Select	NP_004073.2:p.Gly353=
ENST00000628224.3:c.1059C>T MANE Select	ENSP00000487279.2:p.Gly353=
NM_001135040.2:c.999C>T	NP_001128512.1:p.Gly333=
NM_001135040.3:c.999C>T	NP_001128512.1:p.Gly333=
NM_001135041.2:c.657C>T	NP_001128513.1:p.Gly219=
NM_001135041.3:c.657C>T	NP_001128513.1:p.Gly219=
NM_001190836.1:c.948C>T	NP_001177765.1:p.Gly316=
NM_001190836.2:c.948C>T	NP_001177765.1:p.Gly316=
NM_001190837.1:c.1038C>T	NP_001177766.1:p.Gly346=
NM_001190837.2:c.1038C>T	NP_001177766.1:p.Gly346=
NM_001378991.1:c.1008C>T	NP_001365920.1:p.Gly336=
NM_001378992.1:c.990C>T	NP_001365921.1:p.Gly330=
NM_004082.4:c.1059C>T	NP_004073.2:p.Gly353=
NM_023019.3:c.657C>T	NP_075408.1:p.Gly219=
NM_023019.4:c.657C>T	NP_075408.1:p.Gly219=
NR_033935.1:n.1260C>T
NR_033935.2:n.1039C>T
ENST00000361874.7:c.1059C>T	ENSP00000354791.3:p.Gly353=
ENST00000361874.8:c.1059C>T	ENSP00000354791.4:p.Gly353=
ENST00000394003.7:c.1038C>T	ENSP00000377571.3:p.Gly346=
ENST00000409240.5:c.948C>T	ENSP00000386406.1:p.Gly316=
ENST00000409438.5:c.657C>T	ENSP00000387270.1:p.Gly219=
ENST00000409567.7:c.999C>T	ENSP00000386843.3:p.Gly333=
ENST00000409868.5:c.1008C>T	ENSP00000387327.1:p.Gly336=
ENST00000434055.5:c.948C>T	ENSP00000416711.1:p.Gly316=
ENST00000466110.5:n.1280C>T
ENST00000628224.2:c.1008C>T	ENSP00000487279.1:p.Gly336=
ENST00000633691.1:c.657C>T	ENSP00000487724.1:p.Gly219=
ENST00000680606.1:c.1008C>T	ENSP00000505612.1:p.Gly336=