Canonical Allele Identifier: CA7110395

Gene: ACIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23079813G>A , CM000676.2:g.23079813G>A	GRCh38
NC_000014.8:g.23549022G>A , CM000676.1:g.23549022G>A	GRCh37
NC_000014.7:g.22618862G>A	NCBI36
NG_030461.1:g.20802C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000605057.6:c.1522C>T MANE Select	ENSP00000474349.1:p.Pro508Ser
ENST00000262710.5:c.1696C>T	ENSP00000262710.1:p.Pro566Ser
ENST00000457657.5:c.1576C>T	ENSP00000405677.1:p.Pro526Ser
ENST00000555053.5:c.1696C>T	ENSP00000451328.1:p.Pro566Ser
ENST00000605057.5:c.1522C>T	ENSP00000474349.1:p.Pro508Ser
NM_001164814.1:c.1696C>T	NP_001158286.1:p.Pro566Ser
NM_001164815.1:c.1576C>T	NP_001158287.1:p.Pro526Ser
NM_014977.3:c.1696C>T	NP_055792.1:p.Pro566Ser
XM_005267415.2:c.1696C>T	XP_005267472.1:p.Pro566Ser
XM_005267416.2:c.1696C>T	XP_005267473.1:p.Pro566Ser
XM_006720081.2:c.1696C>T	XP_006720144.1:p.Pro566Ser
XM_011536569.1:c.1408C>T	XP_011534871.1:p.Pro470Ser
XM_011536570.1:c.1696C>T	XP_011534872.1:p.Pro566Ser
XR_429297.2:n.1829C>T
XM_005267415.4:c.1696C>T	XP_005267472.1:p.Pro566Ser
XM_005267416.4:c.1696C>T	XP_005267473.1:p.Pro566Ser
XM_006720081.4:c.1696C>T	XP_006720144.1:p.Pro566Ser
XM_011536570.3:c.1696C>T	XP_011534872.1:p.Pro566Ser
XM_024449512.1:c.1576C>T	XP_024305280.1:p.Pro526Ser
XR_429297.4:n.1823C>T
NM_001386863.1:c.1522C>T MANE Select	NP_001373792.1:p.Pro508Ser