Canonical Allele Identifier: CA350469583
Gene: ABCA12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214990974T>C , CM000664.2:g.214990974T>C GRCh38
NC_000002.11:g.215855698T>C , CM000664.1:g.215855698T>C GRCh37
NC_000002.10:g.215563943T>C NCBI36
NG_007074.1:g.152454A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.3352A>G MANE Select ENSP00000272895.7:p.Ser1118Gly
ENST00000272895.11:c.3352A>G ENSP00000272895.7:p.Ser1118Gly
ENST00000389661.4:c.2398A>G ENSP00000374312.4:p.Ser800Gly
NM_015657.3:c.2398A>G NP_056472.2:p.Ser800Gly
NM_173076.2:c.3352A>G NP_775099.2:p.Ser1118Gly
NR_103740.1:n.3652A>G
XM_011510951.1:c.3352A>G XP_011509253.1:p.Ser1118Gly
XM_011510952.1:c.3352A>G XP_011509254.1:p.Ser1118Gly
XM_011510951.2:c.3352A>G XP_011509253.1:p.Ser1118Gly
NM_173076.3:c.3352A>G MANE Select NP_775099.2:p.Ser1118Gly
NR_103740.2:n.3850A>G
NM_015657.4:c.2398A>G NP_056472.2:p.Ser800Gly