Canonical Allele Identifier: CA350793592
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214945022G>A , CM000664.2:g.214945022G>A GRCh38
NC_000002.11:g.215809746G>A , CM000664.1:g.215809746G>A GRCh37
NC_000002.10:g.215517991G>A NCBI36
NG_007074.1:g.198406C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.7322C>T (ABCA12) MANE Select ENSP00000272895.7:p.Ser2441Phe
ENST00000272895.11:c.7322C>T (ABCA12) ENSP00000272895.7:p.Ser2441Phe
ENST00000389661.4:c.6368C>T (ABCA12) ENSP00000374312.4:p.Ser2123Phe
NM_015657.3:c.6368C>T (ABCA12) NP_056472.2:p.Ser2123Phe
NM_173076.2:c.7322C>T (ABCA12) NP_775099.2:p.Ser2441Phe
NR_103740.1:n.7622C>T (ABCA12)
NR_110292.1:n.322-2803G>A (SNHG31)
XM_011510951.1:c.7331C>T (ABCA12) XP_011509253.1:p.Ser2444Phe
XM_011510951.2:c.7331C>T (ABCA12) XP_011509253.1:p.Ser2444Phe
NM_173076.3:c.7322C>T (ABCA12) MANE Select NP_775099.2:p.Ser2441Phe
NR_103740.2:n.7820C>T (ABCA12)
NM_015657.4:c.6368C>T (ABCA12) NP_056472.2:p.Ser2123Phe