Canonical Allele Identifier: CA1327150066

Gene: ABCA12 SNHG31

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214953901A= , CM000664.2:g.214953901A=	GRCh38
NC_000002.11:g.215818625A= , CM000664.1:g.215818625A=	GRCh37
NC_000002.10:g.215526870A=	NCBI36
NG_007074.1:g.189527T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.6600T= (ABCA12) MANE Select	ENSP00000272895.7:p.Phe2200=
ENST00000272895.11:c.6600T= (ABCA12)	ENSP00000272895.7:p.Phe2200=
ENST00000389661.4:c.5646T= (ABCA12)	ENSP00000374312.4:p.Phe1882=
NM_015657.3:c.5646T= (ABCA12)	NP_056472.2:p.Phe1882=
NM_173076.2:c.6600T= (ABCA12)	NP_775099.2:p.Phe2200=
NR_103740.1:n.6900T= (ABCA12)
NR_110292.1:n.444+5954A= (SNHG31)
XM_011510951.1:c.6609T= (ABCA12)	XP_011509253.1:p.Phe2203=
XM_011510951.2:c.6609T= (ABCA12)	XP_011509253.1:p.Phe2203=
NM_173076.3:c.6600T= (ABCA12) MANE Select	NP_775099.2:p.Phe2200=
NR_103740.2:n.7098T= (ABCA12)
NM_015657.4:c.5646T= (ABCA12)	NP_056472.2:p.Phe1882=