Canonical Allele Identifier: CA2662976184
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214953801G>A , CM000664.2:g.214953801G>A GRCh38
NC_000002.11:g.215818525G>A , CM000664.1:g.215818525G>A GRCh37
NC_000002.10:g.215526770G>A NCBI36
NG_007074.1:g.189627C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.6647+53C>T (ABCA12) MANE Select ENSP00000272895.7:n.6647+53C>T
ENST00000272895.11:c.6647+53C>T (ABCA12) ENSP00000272895.7:n.6647+53C>T
ENST00000389661.4:c.5693+53C>T (ABCA12) ENSP00000374312.4:n.5693+53C>T
NM_015657.3:c.5693+53C>T (ABCA12) NP_056472.2:n.5693+53C>T
NM_173076.2:c.6647+53C>T (ABCA12) NP_775099.2:n.6647+53C>T
NR_103740.1:n.6947+53C>T (ABCA12)
NR_110292.1:n.444+5854G>A (SNHG31)
XM_011510951.1:c.6656+53C>T (ABCA12) XP_011509253.1:n.6656+53C>T
XM_011510951.2:c.6656+53C>T (ABCA12) XP_011509253.1:n.6656+53C>T
NM_173076.3:c.6647+53C>T (ABCA12) MANE Select NP_775099.2:n.6647+53C>T
NR_103740.2:n.7145+53C>T (ABCA12)
NM_015657.4:c.5693+53C>T (ABCA12) NP_056472.2:n.5693+53C>T