Canonical Allele Identifier: CA350793619
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.7312A>T (ABCA12) MANE Select ENSP00000272895.7:p.Asn2438Tyr
ENST00000272895.11:c.7312A>T (ABCA12) ENSP00000272895.7:p.Asn2438Tyr
ENST00000389661.4:c.6358A>T (ABCA12) ENSP00000374312.4:p.Asn2120Tyr
NM_015657.3:c.6358A>T (ABCA12) NP_056472.2:p.Asn2120Tyr
NM_173076.2:c.7312A>T (ABCA12) NP_775099.2:p.Asn2438Tyr
NR_103740.1:n.7612A>T (ABCA12)
NR_110292.1:n.322-2793T>A (SNHG31)
XM_011510951.1:c.7321A>T (ABCA12) XP_011509253.1:p.Asn2441Tyr
XM_011510951.2:c.7321A>T (ABCA12) XP_011509253.1:p.Asn2441Tyr
NM_173076.3:c.7312A>T (ABCA12) MANE Select NP_775099.2:p.Asn2438Tyr
NR_103740.2:n.7810A>T (ABCA12)
NM_015657.4:c.6358A>T (ABCA12) NP_056472.2:p.Asn2120Tyr