Canonical Allele Identifier: CA1327150029
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214953821A= , CM000664.2:g.214953821A= GRCh38
NC_000002.11:g.215818545A= , CM000664.1:g.215818545A= GRCh37
NC_000002.10:g.215526790A= NCBI36
NG_007074.1:g.189607T=

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.6647+33T= (ABCA12) MANE Select ENSP00000272895.7:n.6647+33T=
ENST00000272895.11:c.6647+33T= (ABCA12) ENSP00000272895.7:n.6647+33T=
ENST00000389661.4:c.5693+33T= (ABCA12) ENSP00000374312.4:n.5693+33T=
NM_015657.3:c.5693+33T= (ABCA12) NP_056472.2:n.5693+33T=
NM_173076.2:c.6647+33T= (ABCA12) NP_775099.2:n.6647+33T=
NR_103740.1:n.6947+33T= (ABCA12)
NR_110292.1:n.444+5874A= (SNHG31)
XM_011510951.1:c.6656+33T= (ABCA12) XP_011509253.1:n.6656+33T=
XM_011510951.2:c.6656+33T= (ABCA12) XP_011509253.1:n.6656+33T=
NM_173076.3:c.6647+33T= (ABCA12) MANE Select NP_775099.2:n.6647+33T=
NR_103740.2:n.7145+33T= (ABCA12)
NM_015657.4:c.5693+33T= (ABCA12) NP_056472.2:n.5693+33T=