Canonical Allele Identifier: CA350460701
Gene: ABCA12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214980499G>T , CM000664.2:g.214980499G>T GRCh38
NC_000002.11:g.215845223G>T , CM000664.1:g.215845223G>T GRCh37
NC_000002.10:g.215553468G>T NCBI36
NG_007074.1:g.162929C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.4724C>A MANE Select ENSP00000272895.7:p.Thr1575Lys
ENST00000272895.11:c.4724C>A ENSP00000272895.7:p.Thr1575Lys
ENST00000389661.4:c.3770C>A ENSP00000374312.4:p.Thr1257Lys
NM_015657.3:c.3770C>A NP_056472.2:p.Thr1257Lys
NM_173076.2:c.4724C>A NP_775099.2:p.Thr1575Lys
NR_103740.1:n.5024C>A
XM_011510951.1:c.4733C>A XP_011509253.1:p.Thr1578Lys
XM_011510952.1:c.4733C>A XP_011509254.1:p.Thr1578Lys
XM_011510951.2:c.4733C>A XP_011509253.1:p.Thr1578Lys
NM_173076.3:c.4724C>A MANE Select NP_775099.2:p.Thr1575Lys
NR_103740.2:n.5222C>A
NM_015657.4:c.3770C>A NP_056472.2:p.Thr1257Lys