Canonical Allele Identifier: CA1327146206
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214945032T= , CM000664.2:g.214945032T= GRCh38
NC_000002.11:g.215809756T= , CM000664.1:g.215809756T= GRCh37
NC_000002.10:g.215518001T= NCBI36
NG_007074.1:g.198396A=

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.7312A= (ABCA12) MANE Select ENSP00000272895.7:p.Asn2438=
ENST00000272895.11:c.7312A= (ABCA12) ENSP00000272895.7:p.Asn2438=
ENST00000389661.4:c.6358A= (ABCA12) ENSP00000374312.4:p.Asn2120=
NM_015657.3:c.6358A= (ABCA12) NP_056472.2:p.Asn2120=
NM_173076.2:c.7312A= (ABCA12) NP_775099.2:p.Asn2438=
NR_103740.1:n.7612A= (ABCA12)
NR_110292.1:n.322-2793T= (SNHG31)
XM_011510951.1:c.7321A= (ABCA12) XP_011509253.1:p.Asn2441=
XM_011510951.2:c.7321A= (ABCA12) XP_011509253.1:p.Asn2441=
NM_173076.3:c.7312A= (ABCA12) MANE Select NP_775099.2:p.Asn2438=
NR_103740.2:n.7810A= (ABCA12)
NM_015657.4:c.6358A= (ABCA12) NP_056472.2:p.Asn2120=