Canonical Allele Identifier: CA1261398957

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74378079C= , CM000664.2:g.74378079C=	GRCh38
NC_000002.11:g.74605206C= , CM000664.1:g.74605206C=	GRCh37
NC_000002.10:g.74458714C=	NCBI36
NG_008735.2:g.19009G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361874.8:c.200G=	ENSP00000354791.4:p.Gly67=
ENST00000628224.3:c.200G= MANE Select	ENSP00000487279.2:p.Gly67=
ENST00000680606.1:c.149G=	ENSP00000505612.1:p.Gly50=
ENST00000361874.7:c.200G=	ENSP00000354791.3:p.Gly67=
ENST00000394003.7:c.200G=	ENSP00000377571.3:p.Gly67=
ENST00000409240.5:c.149G=	ENSP00000386406.1:p.Gly50=
ENST00000409567.7:c.200G=	ENSP00000386843.3:p.Gly67=
ENST00000409868.5:c.149G=	ENSP00000387327.1:p.Gly50=
ENST00000413111.5:c.149G=	ENSP00000413268.1:p.Gly50=
ENST00000417090.1:c.212G=	ENSP00000402509.1:p.Gly71=
ENST00000421392.1:c.149G=	ENSP00000409363.1:p.Gly50=
ENST00000434055.5:c.149G=	ENSP00000416711.1:p.Gly50=
ENST00000437375.1:c.149G=	ENSP00000395312.1:p.Gly50=
ENST00000440727.1:c.149G=	ENSP00000400059.1:p.Gly50=
ENST00000454119.5:c.149G=	ENSP00000404038.1:p.Gly50=
ENST00000458655.5:c.221G=	ENSP00000414315.1:p.Gly74=
ENST00000628224.2:c.149G=	ENSP00000487279.1:p.Gly50=
NM_001135040.2:c.200G=	NP_001128512.1:p.Gly67=
NM_001190836.1:c.149G=	NP_001177765.1:p.Gly50=
NM_001190837.1:c.200G=	NP_001177766.1:p.Gly67=
NM_004082.4:c.200G=	NP_004073.2:p.Gly67=
NR_033935.1:n.461G=
NM_001135040.3:c.200G=	NP_001128512.1:p.Gly67=
NM_001190836.2:c.149G=	NP_001177765.1:p.Gly50=
NM_001190837.2:c.200G=	NP_001177766.1:p.Gly67=
NM_001378991.1:c.149G=	NP_001365920.1:p.Gly50=
NM_001378992.1:c.149G=	NP_001365921.1:p.Gly50=
NM_004082.5:c.200G= MANE Select	NP_004073.2:p.Gly67=
NR_033935.2:n.240G=