Canonical Allele Identifier: CA431151438

Gene: ABCA12

Linked Data

• MyVariant Identifiers: chr2:g.215876218A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215011494A>C , CM000664.2:g.215011494A>C	GRCh38
NC_000002.11:g.215876218A>C , CM000664.1:g.215876218A>C	GRCh37
NC_000002.10:g.215584463A>C	NCBI36
NG_007074.1:g.131934T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.2277T>G MANE Select	ENSP00000272895.7:p.Thr759=
ENST00000272895.11:c.2277T>G	ENSP00000272895.7:p.Thr759=
ENST00000389661.4:c.1323T>G	ENSP00000374312.4:p.Thr441=
NM_015657.3:c.1323T>G	NP_056472.2:p.Thr441=
NM_173076.2:c.2277T>G	NP_775099.2:p.Thr759=
NR_103740.1:n.2521T>G
XM_011510951.1:c.2277T>G	XP_011509253.1:p.Thr759=
XM_011510952.1:c.2277T>G	XP_011509254.1:p.Thr759=
XM_011510951.2:c.2277T>G	XP_011509253.1:p.Thr759=
NM_173076.3:c.2277T>G MANE Select	NP_775099.2:p.Thr759=
NR_103740.2:n.2719T>G
NM_015657.4:c.1323T>G	NP_056472.2:p.Thr441=