Canonical Allele Identifier: CA350459439

Gene: ABCA12

Linked Data

• MyVariant Identifiers: chr2:g.215843530C>A (hg19) ; chr2:g.214978806C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214978806C>A , CM000664.2:g.214978806C>A	GRCh38
NC_000002.11:g.215843530C>A , CM000664.1:g.215843530C>A	GRCh37
NC_000002.10:g.215551775C>A	NCBI36
NG_007074.1:g.164622G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.4975G>T MANE Select	ENSP00000272895.7:p.Glu1659Ter
ENST00000272895.11:c.4975G>T	ENSP00000272895.7:p.Glu1659Ter
ENST00000389661.4:c.4021G>T	ENSP00000374312.4:p.Glu1341Ter
NM_015657.3:c.4021G>T	NP_056472.2:p.Glu1341Ter
NM_173076.2:c.4975G>T	NP_775099.2:p.Glu1659Ter
NR_103740.1:n.5275G>T
XM_011510951.1:c.4984G>T	XP_011509253.1:p.Glu1662Ter
XM_011510952.1:c.4984G>T	XP_011509254.1:p.Glu1662Ter
XM_011510951.2:c.4984G>T	XP_011509253.1:p.Glu1662Ter
NM_173076.3:c.4975G>T MANE Select	NP_775099.2:p.Glu1659Ter
NR_103740.2:n.5473G>T
NM_015657.4:c.4021G>T	NP_056472.2:p.Glu1341Ter