Canonical Allele Identifier: CA431148765

Gene: ABCA12

Linked Data

• gnomAD v4: 2-214980549-A-G
• MyVariant Identifiers: chr2:g.215845273A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214980549A>G , CM000664.2:g.214980549A>G	GRCh38
NC_000002.11:g.215845273A>G , CM000664.1:g.215845273A>G	GRCh37
NC_000002.10:g.215553518A>G	NCBI36
NG_007074.1:g.162879T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.4674T>C MANE Select	ENSP00000272895.7:p.Cys1558=
ENST00000272895.11:c.4674T>C	ENSP00000272895.7:p.Cys1558=
ENST00000389661.4:c.3720T>C	ENSP00000374312.4:p.Cys1240=
NM_015657.3:c.3720T>C	NP_056472.2:p.Cys1240=
NM_173076.2:c.4674T>C	NP_775099.2:p.Cys1558=
NR_103740.1:n.4974T>C
XM_011510951.1:c.4683T>C	XP_011509253.1:p.Cys1561=
XM_011510952.1:c.4683T>C	XP_011509254.1:p.Cys1561=
XM_011510951.2:c.4683T>C	XP_011509253.1:p.Cys1561=
NM_173076.3:c.4674T>C MANE Select	NP_775099.2:p.Cys1558=
NR_103740.2:n.5172T>C
NM_015657.4:c.3720T>C	NP_056472.2:p.Cys1240=