Canonical Allele Identifier: CA7110408

Gene: ACIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23079905T>C , CM000676.2:g.23079905T>C	GRCh38
NC_000014.8:g.23549114T>C , CM000676.1:g.23549114T>C	GRCh37
NC_000014.7:g.22618954T>C	NCBI36
NG_030461.1:g.20710A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000605057.6:c.1430A>G MANE Select	ENSP00000474349.1:p.Glu477Gly
ENST00000262710.5:c.1604A>G	ENSP00000262710.1:p.Glu535Gly
ENST00000457657.5:c.1484A>G	ENSP00000405677.1:p.Glu495Gly
ENST00000555053.5:c.1604A>G	ENSP00000451328.1:p.Glu535Gly
ENST00000605057.5:c.1430A>G	ENSP00000474349.1:p.Glu477Gly
NM_001164814.1:c.1604A>G	NP_001158286.1:p.Glu535Gly
NM_001164815.1:c.1484A>G	NP_001158287.1:p.Glu495Gly
NM_014977.3:c.1604A>G	NP_055792.1:p.Glu535Gly
XM_005267415.2:c.1604A>G	XP_005267472.1:p.Glu535Gly
XM_005267416.2:c.1604A>G	XP_005267473.1:p.Glu535Gly
XM_006720081.2:c.1604A>G	XP_006720144.1:p.Glu535Gly
XM_011536569.1:c.1316A>G	XP_011534871.1:p.Glu439Gly
XM_011536570.1:c.1604A>G	XP_011534872.1:p.Glu535Gly
XR_429297.2:n.1737A>G
XM_005267415.4:c.1604A>G	XP_005267472.1:p.Glu535Gly
XM_005267416.4:c.1604A>G	XP_005267473.1:p.Glu535Gly
XM_006720081.4:c.1604A>G	XP_006720144.1:p.Glu535Gly
XM_011536570.3:c.1604A>G	XP_011534872.1:p.Glu535Gly
XM_024449512.1:c.1484A>G	XP_024305280.1:p.Glu495Gly
XR_429297.4:n.1731A>G
NM_001386863.1:c.1430A>G MANE Select	NP_001373792.1:p.Glu477Gly