Canonical Allele Identifier: CA350460790

Gene: ABCA12

Linked Data

• gnomAD v4: 2-214980520-A-C
• MyVariant Identifiers: chr2:g.215845244A>C (hg19) ; chr2:g.214980520A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214980520A>C , CM000664.2:g.214980520A>C	GRCh38
NC_000002.11:g.215845244A>C , CM000664.1:g.215845244A>C	GRCh37
NC_000002.10:g.215553489A>C	NCBI36
NG_007074.1:g.162908T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.4703T>G MANE Select	ENSP00000272895.7:p.Phe1568Cys
ENST00000272895.11:c.4703T>G	ENSP00000272895.7:p.Phe1568Cys
ENST00000389661.4:c.3749T>G	ENSP00000374312.4:p.Phe1250Cys
NM_015657.3:c.3749T>G	NP_056472.2:p.Phe1250Cys
NM_173076.2:c.4703T>G	NP_775099.2:p.Phe1568Cys
NR_103740.1:n.5003T>G
XM_011510951.1:c.4712T>G	XP_011509253.1:p.Phe1571Cys
XM_011510952.1:c.4712T>G	XP_011509254.1:p.Phe1571Cys
XM_011510951.2:c.4712T>G	XP_011509253.1:p.Phe1571Cys
NM_173076.3:c.4703T>G MANE Select	NP_775099.2:p.Phe1568Cys
NR_103740.2:n.5201T>G
NM_015657.4:c.3749T>G	NP_056472.2:p.Phe1250Cys