Canonical Allele Identifier: CA350446037

Gene: ABCA12 SNHG31

Linked Data

• MyVariant Identifiers: chr2:g.215818615G>C (hg19) ; chr2:g.214953891G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214953891G>C , CM000664.2:g.214953891G>C	GRCh38
NC_000002.11:g.215818615G>C , CM000664.1:g.215818615G>C	GRCh37
NC_000002.10:g.215526860G>C	NCBI36
NG_007074.1:g.189537C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.6610C>G (ABCA12) MANE Select	ENSP00000272895.7:p.Arg2204Gly
ENST00000272895.11:c.6610C>G (ABCA12)	ENSP00000272895.7:p.Arg2204Gly
ENST00000389661.4:c.5656C>G (ABCA12)	ENSP00000374312.4:p.Arg1886Gly
NM_015657.3:c.5656C>G (ABCA12)	NP_056472.2:p.Arg1886Gly
NM_173076.2:c.6610C>G (ABCA12)	NP_775099.2:p.Arg2204Gly
NR_103740.1:n.6910C>G (ABCA12)
NR_110292.1:n.444+5944G>C (SNHG31)
XM_011510951.1:c.6619C>G (ABCA12)	XP_011509253.1:p.Arg2207Gly
XM_011510951.2:c.6619C>G (ABCA12)	XP_011509253.1:p.Arg2207Gly
NM_173076.3:c.6610C>G (ABCA12) MANE Select	NP_775099.2:p.Arg2204Gly
NR_103740.2:n.7108C>G (ABCA12)
NM_015657.4:c.5656C>G (ABCA12)	NP_056472.2:p.Arg1886Gly