Canonical Allele Identifier: CA350446075

Gene: ABCA12 SNHG31

Linked Data

• MyVariant Identifiers: chr2:g.215818633T>A (hg19) ; chr2:g.214953909T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214953909T>A , CM000664.2:g.214953909T>A	GRCh38
NC_000002.11:g.215818633T>A , CM000664.1:g.215818633T>A	GRCh37
NC_000002.10:g.215526878T>A	NCBI36
NG_007074.1:g.189519A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.6592A>T (ABCA12) MANE Select	ENSP00000272895.7:p.Thr2198Ser
ENST00000272895.11:c.6592A>T (ABCA12)	ENSP00000272895.7:p.Thr2198Ser
ENST00000389661.4:c.5638A>T (ABCA12)	ENSP00000374312.4:p.Thr1880Ser
NM_015657.3:c.5638A>T (ABCA12)	NP_056472.2:p.Thr1880Ser
NM_173076.2:c.6592A>T (ABCA12)	NP_775099.2:p.Thr2198Ser
NR_103740.1:n.6892A>T (ABCA12)
NR_110292.1:n.444+5962T>A (SNHG31)
XM_011510951.1:c.6601A>T (ABCA12)	XP_011509253.1:p.Thr2201Ser
XM_011510951.2:c.6601A>T (ABCA12)	XP_011509253.1:p.Thr2201Ser
NM_173076.3:c.6592A>T (ABCA12) MANE Select	NP_775099.2:p.Thr2198Ser
NR_103740.2:n.7090A>T (ABCA12)
NM_015657.4:c.5638A>T (ABCA12)	NP_056472.2:p.Thr1880Ser