Canonical Allele Identifier: CA1327196921
Gene: ABCA12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064013A= , CM000664.2:g.215064013A= GRCh38
NC_000002.11:g.215928736A= , CM000664.1:g.215928736A= GRCh37
NC_000002.10:g.215636981A= NCBI36
NG_007074.1:g.79416T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.317+53T= MANE Select ENSP00000272895.7:n.317+53T=
ENST00000272895.11:c.317+53T= ENSP00000272895.7:n.317+53T=
NM_173076.2:c.317+53T= NP_775099.2:n.317+53T=
NR_103740.1:n.537+53T=
XM_011510951.1:c.317+53T= XP_011509253.1:n.317+53T=
XM_011510952.1:c.317+53T= XP_011509254.1:n.317+53T=
XM_011510951.2:c.317+53T= XP_011509253.1:n.317+53T=
NM_173076.3:c.317+53T= MANE Select NP_775099.2:n.317+53T=
NR_103740.2:n.735+53T=