Canonical Allele Identifier: CA1721950

Gene: DCTN1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74367744A>G , CM000664.2:g.74367744A>G	GRCh38
NC_000002.11:g.74594871A>G , CM000664.1:g.74594871A>G	GRCh37
NC_000002.10:g.74448379A>G	NCBI36
NG_008735.2:g.29344T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361874.8:c.2136T>C	ENSP00000354791.4:p.Asp712=
ENST00000628224.3:c.2136T>C MANE Select	ENSP00000487279.2:p.Asp712=
ENST00000680606.1:c.2085T>C	ENSP00000505612.1:p.Asp695=
ENST00000361874.7:c.2136T>C	ENSP00000354791.3:p.Asp712=
ENST00000394003.7:c.2115T>C	ENSP00000377571.3:p.Asp705=
ENST00000409240.5:c.2025T>C	ENSP00000386406.1:p.Asp675=
ENST00000409438.5:c.1734T>C	ENSP00000387270.1:p.Asp578=
ENST00000409567.7:c.2076T>C	ENSP00000386843.3:p.Asp692=
ENST00000409868.5:c.2085T>C	ENSP00000387327.1:p.Asp695=
ENST00000434055.5:c.2025T>C	ENSP00000416711.1:p.Asp675=
ENST00000466110.5:n.2953T>C
ENST00000495643.1:n.164T>C
ENST00000497666.1:n.96+1556T>C
ENST00000628224.2:c.2085T>C	ENSP00000487279.1:p.Asp695=
ENST00000633691.1:c.1734T>C	ENSP00000487724.1:p.Asp578=
NM_001135040.2:c.2076T>C	NP_001128512.1:p.Asp692=
NM_001135041.2:c.1734T>C	NP_001128513.1:p.Asp578=
NM_001190836.1:c.2025T>C	NP_001177765.1:p.Asp675=
NM_001190837.1:c.2115T>C	NP_001177766.1:p.Asp705=
NM_004082.4:c.2136T>C	NP_004073.2:p.Asp712=
NM_023019.3:c.1734T>C	NP_075408.1:p.Asp578=
NR_033935.1:n.2337T>C
NM_001135040.3:c.2076T>C	NP_001128512.1:p.Asp692=
NM_001135041.3:c.1734T>C	NP_001128513.1:p.Asp578=
NM_001190836.2:c.2025T>C	NP_001177765.1:p.Asp675=
NM_001190837.2:c.2115T>C	NP_001177766.1:p.Asp705=
NM_001378991.1:c.2085T>C	NP_001365920.1:p.Asp695=
NM_001378992.1:c.2067T>C	NP_001365921.1:p.Asp689=
NM_004082.5:c.2136T>C MANE Select	NP_004073.2:p.Asp712=
NM_023019.4:c.1734T>C	NP_075408.1:p.Asp578=
NR_033935.2:n.2116T>C