Canonical Allele Identifier: CA350792883
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214937520G>C , CM000664.2:g.214937520G>C GRCh38
NC_000002.11:g.215802244G>C , CM000664.1:g.215802244G>C GRCh37
NC_000002.10:g.215510489G>C NCBI36
NG_007074.1:g.205908C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.7532C>G (ABCA12) MANE Select ENSP00000272895.7:p.Thr2511Arg
ENST00000272895.11:c.7532C>G (ABCA12) ENSP00000272895.7:p.Thr2511Arg
ENST00000389661.4:c.6578C>G (ABCA12) ENSP00000374312.4:p.Thr2193Arg
NM_015657.3:c.6578C>G (ABCA12) NP_056472.2:p.Thr2193Arg
NM_173076.2:c.7532C>G (ABCA12) NP_775099.2:p.Thr2511Arg
NR_103740.1:n.7832C>G (ABCA12)
NR_110292.1:n.322-10305G>C (SNHG31)
XM_011510951.1:c.7541C>G (ABCA12) XP_011509253.1:p.Thr2514Arg
XM_011510951.2:c.7541C>G (ABCA12) XP_011509253.1:p.Thr2514Arg
NM_173076.3:c.7532C>G (ABCA12) MANE Select NP_775099.2:p.Thr2511Arg
NR_103740.2:n.8030C>G (ABCA12)
NM_015657.4:c.6578C>G (ABCA12) NP_056472.2:p.Thr2193Arg