Canonical Allele Identifier: CA350792873
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214937515A>T , CM000664.2:g.214937515A>T GRCh38
NC_000002.11:g.215802239A>T , CM000664.1:g.215802239A>T GRCh37
NC_000002.10:g.215510484A>T NCBI36
NG_007074.1:g.205913T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.7537T>A (ABCA12) MANE Select ENSP00000272895.7:p.Leu2513Ile
ENST00000272895.11:c.7537T>A (ABCA12) ENSP00000272895.7:p.Leu2513Ile
ENST00000389661.4:c.6583T>A (ABCA12) ENSP00000374312.4:p.Leu2195Ile
NM_015657.3:c.6583T>A (ABCA12) NP_056472.2:p.Leu2195Ile
NM_173076.2:c.7537T>A (ABCA12) NP_775099.2:p.Leu2513Ile
NR_103740.1:n.7837T>A (ABCA12)
NR_110292.1:n.322-10310A>T (SNHG31)
XM_011510951.1:c.7546T>A (ABCA12) XP_011509253.1:p.Leu2516Ile
XM_011510951.2:c.7546T>A (ABCA12) XP_011509253.1:p.Leu2516Ile
NM_173076.3:c.7537T>A (ABCA12) MANE Select NP_775099.2:p.Leu2513Ile
NR_103740.2:n.8035T>A (ABCA12)
NM_015657.4:c.6583T>A (ABCA12) NP_056472.2:p.Leu2195Ile