Canonical Allele Identifier: CA350460744

Gene: ABCA12

Linked Data

• MyVariant Identifiers: chr2:g.215845233A>C (hg19) ; chr2:g.214980509A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214980509A>C , CM000664.2:g.214980509A>C	GRCh38
NC_000002.11:g.215845233A>C , CM000664.1:g.215845233A>C	GRCh37
NC_000002.10:g.215553478A>C	NCBI36
NG_007074.1:g.162919T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.4714T>G MANE Select	ENSP00000272895.7:p.Tyr1572Asp
ENST00000272895.11:c.4714T>G	ENSP00000272895.7:p.Tyr1572Asp
ENST00000389661.4:c.3760T>G	ENSP00000374312.4:p.Tyr1254Asp
NM_015657.3:c.3760T>G	NP_056472.2:p.Tyr1254Asp
NM_173076.2:c.4714T>G	NP_775099.2:p.Tyr1572Asp
NR_103740.1:n.5014T>G
XM_011510951.1:c.4723T>G	XP_011509253.1:p.Tyr1575Asp
XM_011510952.1:c.4723T>G	XP_011509254.1:p.Tyr1575Asp
XM_011510951.2:c.4723T>G	XP_011509253.1:p.Tyr1575Asp
NM_173076.3:c.4714T>G MANE Select	NP_775099.2:p.Tyr1572Asp
NR_103740.2:n.5212T>G
NM_015657.4:c.3760T>G	NP_056472.2:p.Tyr1254Asp