Canonical Allele Identifier: CA1327141176

Gene: ABCA12 SNHG31

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214932673A= , CM000664.2:g.214932673A=	GRCh38
NC_000002.11:g.215797397A= , CM000664.1:g.215797397A=	GRCh37
NC_000002.10:g.215505642A=	NCBI36
NG_007074.1:g.210755T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.7749T= (ABCA12) MANE Select	ENSP00000272895.7:p.Thr2583=
ENST00000272895.11:c.7749T= (ABCA12)	ENSP00000272895.7:p.Thr2583=
ENST00000389661.4:c.6795T= (ABCA12)	ENSP00000374312.4:p.Thr2265=
NM_015657.3:c.6795T= (ABCA12)	NP_056472.2:p.Thr2265=
NM_173076.2:c.7749T= (ABCA12)	NP_775099.2:p.Thr2583=
NR_103740.1:n.8049T= (ABCA12)
NR_110292.1:n.322-15152A= (SNHG31)
XM_011510951.1:c.7758T= (ABCA12)	XP_011509253.1:p.Thr2586=
XM_011510951.2:c.7758T= (ABCA12)	XP_011509253.1:p.Thr2586=
NM_173076.3:c.7749T= (ABCA12) MANE Select	NP_775099.2:p.Thr2583=
NR_103740.2:n.8247T= (ABCA12)
NM_015657.4:c.6795T= (ABCA12)	NP_056472.2:p.Thr2265=