Canonical Allele Identifier: CA2577235654
Gene: ABCA12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064022T>G , CM000664.2:g.215064022T>G GRCh38
NC_000002.11:g.215928745T>G , CM000664.1:g.215928745T>G GRCh37
NC_000002.10:g.215636990T>G NCBI36
NG_007074.1:g.79407A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.317+44A>C MANE Select ENSP00000272895.7:n.317+44A>C
ENST00000272895.11:c.317+44A>C ENSP00000272895.7:n.317+44A>C
NM_173076.2:c.317+44A>C NP_775099.2:n.317+44A>C
NR_103740.1:n.537+44A>C
XM_011510951.1:c.317+44A>C XP_011509253.1:n.317+44A>C
XM_011510952.1:c.317+44A>C XP_011509254.1:n.317+44A>C
XM_011510951.2:c.317+44A>C XP_011509253.1:n.317+44A>C
NM_173076.3:c.317+44A>C MANE Select NP_775099.2:n.317+44A>C
NR_103740.2:n.735+44A>C