Canonical Allele Identifier: CA2662973801
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214932064C>A , CM000664.2:g.214932064C>A GRCh38
NC_000002.11:g.215796788C>A , CM000664.1:g.215796788C>A GRCh37
NC_000002.10:g.215505033C>A NCBI36
NG_007074.1:g.211364G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.*570G>T (ABCA12) MANE Select ENSP00000272895.7:n.*570G>T
ENST00000272895.11:c.*570G>T (ABCA12) ENSP00000272895.7:n.*570G>T
NM_015657.3:c.*570G>T (ABCA12) NP_056472.2:n.*570G>T
NM_173076.2:c.*570G>T (ABCA12) NP_775099.2:n.*570G>T
NR_103740.1:n.8658G>T (ABCA12)
NR_110292.1:n.322-15761C>A (SNHG31)
XM_011510951.1:c.*570G>T (ABCA12) XP_011509253.1:n.*570G>T
XM_011510951.2:c.*570G>T (ABCA12) XP_011509253.1:n.*570G>T
NM_173076.3:c.*570G>T (ABCA12) MANE Select NP_775099.2:n.*570G>T
NR_103740.2:n.8856G>T (ABCA12)
NM_015657.4:c.*570G>T (ABCA12) NP_056472.2:n.*570G>T