Canonical Allele Identifier: CA350461134

Gene: ABCA12

Linked Data

• MyVariant Identifiers: chr2:g.215845324T>G (hg19) ; chr2:g.214980600T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214980600T>G , CM000664.2:g.214980600T>G	GRCh38
NC_000002.11:g.215845324T>G , CM000664.1:g.215845324T>G	GRCh37
NC_000002.10:g.215553569T>G	NCBI36
NG_007074.1:g.162828A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.4623A>C MANE Select	ENSP00000272895.7:p.Glu1541Asp
ENST00000272895.11:c.4623A>C	ENSP00000272895.7:p.Glu1541Asp
ENST00000389661.4:c.3669A>C	ENSP00000374312.4:p.Glu1223Asp
NM_015657.3:c.3669A>C	NP_056472.2:p.Glu1223Asp
NM_173076.2:c.4623A>C	NP_775099.2:p.Glu1541Asp
NR_103740.1:n.4923A>C
XM_011510951.1:c.4632A>C	XP_011509253.1:p.Glu1544Asp
XM_011510952.1:c.4632A>C	XP_011509254.1:p.Glu1544Asp
XM_011510951.2:c.4632A>C	XP_011509253.1:p.Glu1544Asp
NM_173076.3:c.4623A>C MANE Select	NP_775099.2:p.Glu1541Asp
NR_103740.2:n.5121A>C
NM_015657.4:c.3669A>C	NP_056472.2:p.Glu1223Asp