Canonical Allele Identifier: CA350793622
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214945034T>A , CM000664.2:g.214945034T>A GRCh38
NC_000002.11:g.215809758T>A , CM000664.1:g.215809758T>A GRCh37
NC_000002.10:g.215518003T>A NCBI36
NG_007074.1:g.198394A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.7310A>T (ABCA12) MANE Select ENSP00000272895.7:p.Gln2437Leu
ENST00000272895.11:c.7310A>T (ABCA12) ENSP00000272895.7:p.Gln2437Leu
ENST00000389661.4:c.6356A>T (ABCA12) ENSP00000374312.4:p.Gln2119Leu
NM_015657.3:c.6356A>T (ABCA12) NP_056472.2:p.Gln2119Leu
NM_173076.2:c.7310A>T (ABCA12) NP_775099.2:p.Gln2437Leu
NR_103740.1:n.7610A>T (ABCA12)
NR_110292.1:n.322-2791T>A (SNHG31)
XM_011510951.1:c.7319A>T (ABCA12) XP_011509253.1:p.Gln2440Leu
XM_011510951.2:c.7319A>T (ABCA12) XP_011509253.1:p.Gln2440Leu
NM_173076.3:c.7310A>T (ABCA12) MANE Select NP_775099.2:p.Gln2437Leu
NR_103740.2:n.7808A>T (ABCA12)
NM_015657.4:c.6356A>T (ABCA12) NP_056472.2:p.Gln2119Leu