Canonical Allele Identifier: CA1261394547

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74368870A= , CM000664.2:g.74368870A=	GRCh38
NC_000002.11:g.74595997A= , CM000664.1:g.74595997A=	GRCh37
NC_000002.10:g.74449505A=	NCBI36
NG_008735.2:g.28218T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361874.8:c.1712T=	ENSP00000354791.4:p.Met571=
ENST00000628224.3:c.1712T= MANE Select	ENSP00000487279.2:p.Met571=
ENST00000680606.1:c.1661T=	ENSP00000505612.1:p.Met554=
ENST00000361874.7:c.1712T=	ENSP00000354791.3:p.Met571=
ENST00000394003.7:c.1691T=	ENSP00000377571.3:p.Met564=
ENST00000409240.5:c.1601T=	ENSP00000386406.1:p.Met534=
ENST00000409438.5:c.1310T=	ENSP00000387270.1:p.Met437=
ENST00000409567.7:c.1652T=	ENSP00000386843.3:p.Met551=
ENST00000409868.5:c.1661T=	ENSP00000387327.1:p.Met554=
ENST00000434055.5:c.1601T=	ENSP00000416711.1:p.Met534=
ENST00000466110.5:n.1933T=
ENST00000497666.1:n.96+430T=
ENST00000628224.2:c.1661T=	ENSP00000487279.1:p.Met554=
ENST00000633691.1:c.1310T=	ENSP00000487724.1:p.Met437=
NM_001135040.2:c.1652T=	NP_001128512.1:p.Met551=
NM_001135041.2:c.1310T=	NP_001128513.1:p.Met437=
NM_001190836.1:c.1601T=	NP_001177765.1:p.Met534=
NM_001190837.1:c.1691T=	NP_001177766.1:p.Met564=
NM_004082.4:c.1712T=	NP_004073.2:p.Met571=
NM_023019.3:c.1310T=	NP_075408.1:p.Met437=
NR_033935.1:n.1913T=
NM_001135040.3:c.1652T=	NP_001128512.1:p.Met551=
NM_001135041.3:c.1310T=	NP_001128513.1:p.Met437=
NM_001190836.2:c.1601T=	NP_001177765.1:p.Met534=
NM_001190837.2:c.1691T=	NP_001177766.1:p.Met564=
NM_001378991.1:c.1661T=	NP_001365920.1:p.Met554=
NM_001378992.1:c.1643T=	NP_001365921.1:p.Met548=
NM_004082.5:c.1712T= MANE Select	NP_004073.2:p.Met571=
NM_023019.4:c.1310T=	NP_075408.1:p.Met437=
NR_033935.2:n.1692T=