Canonical Allele Identifier: CA7110286

Gene: ACIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23078878C>T , CM000676.2:g.23078878C>T	GRCh38
NC_000014.8:g.23548087C>T , CM000676.1:g.23548087C>T	GRCh37
NC_000014.7:g.22617927C>T	NCBI36
NG_030461.1:g.21737G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000605057.6:c.1949G>A MANE Select	ENSP00000474349.1:p.Arg650His
ENST00000262710.5:c.2123G>A	ENSP00000262710.1:p.Arg708His
ENST00000457657.5:c.2003G>A	ENSP00000405677.1:p.Arg668His
ENST00000554708.1:n.208G>A
ENST00000555053.5:c.2123G>A	ENSP00000451328.1:p.Arg708His
ENST00000605057.5:c.1949G>A	ENSP00000474349.1:p.Arg650His
NM_001164814.1:c.2123G>A	NP_001158286.1:p.Arg708His
NM_001164815.1:c.2003G>A	NP_001158287.1:p.Arg668His
NM_014977.3:c.2123G>A	NP_055792.1:p.Arg708His
XM_005267415.2:c.2123G>A	XP_005267472.1:p.Arg708His
XM_005267416.2:c.2123G>A	XP_005267473.1:p.Arg708His
XM_006720081.2:c.2123G>A	XP_006720144.1:p.Arg708His
XM_011536569.1:c.1835G>A	XP_011534871.1:p.Arg612His
XM_011536570.1:c.2123G>A	XP_011534872.1:p.Arg708His
XR_429297.2:n.2256G>A
XM_005267415.4:c.2123G>A	XP_005267472.1:p.Arg708His
XM_005267416.4:c.2123G>A	XP_005267473.1:p.Arg708His
XM_006720081.4:c.2123G>A	XP_006720144.1:p.Arg708His
XM_011536570.3:c.2123G>A	XP_011534872.1:p.Arg708His
XM_024449512.1:c.2003G>A	XP_024305280.1:p.Arg668His
XR_429297.4:n.2250G>A
NM_001386863.1:c.1949G>A MANE Select	NP_001373792.1:p.Arg650His