Canonical Allele Identifier: CA431151411

Gene: ABCA12

Linked Data

• MyVariant Identifiers: chr2:g.215876170T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215011446T>A , CM000664.2:g.215011446T>A	GRCh38
NC_000002.11:g.215876170T>A , CM000664.1:g.215876170T>A	GRCh37
NC_000002.10:g.215584415T>A	NCBI36
NG_007074.1:g.131982A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.2325A>T MANE Select	ENSP00000272895.7:p.Ile775=
ENST00000272895.11:c.2325A>T	ENSP00000272895.7:p.Ile775=
ENST00000389661.4:c.1371A>T	ENSP00000374312.4:p.Ile457=
NM_015657.3:c.1371A>T	NP_056472.2:p.Ile457=
NM_173076.2:c.2325A>T	NP_775099.2:p.Ile775=
NR_103740.1:n.2569A>T
XM_011510951.1:c.2325A>T	XP_011509253.1:p.Ile775=
XM_011510952.1:c.2325A>T	XP_011509254.1:p.Ile775=
XM_011510951.2:c.2325A>T	XP_011509253.1:p.Ile775=
NM_173076.3:c.2325A>T MANE Select	NP_775099.2:p.Ile775=
NR_103740.2:n.2767A>T
NM_015657.4:c.1371A>T	NP_056472.2:p.Ile457=