Canonical Allele Identifier: CA350483570
Gene: ABCA12 HGNC NCBI

Linked Data

dbSNP Id: rs1389966044

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215011523T>C , CM000664.2:g.215011523T>C GRCh38
NC_000002.11:g.215876247T>C , CM000664.1:g.215876247T>C GRCh37
NC_000002.10:g.215584492T>C NCBI36
NG_007074.1:g.131905A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.2248A>G MANE Select ENSP00000272895.7:p.Lys750Glu
ENST00000272895.11:c.2248A>G ENSP00000272895.7:p.Lys750Glu
ENST00000389661.4:c.1294A>G ENSP00000374312.4:p.Lys432Glu
NM_015657.3:c.1294A>G NP_056472.2:p.Lys432Glu
NM_173076.2:c.2248A>G NP_775099.2:p.Lys750Glu
NR_103740.1:n.2492A>G
XM_011510951.1:c.2248A>G XP_011509253.1:p.Lys750Glu
XM_011510952.1:c.2248A>G XP_011509254.1:p.Lys750Glu
XM_011510951.2:c.2248A>G XP_011509253.1:p.Lys750Glu
NM_173076.3:c.2248A>G MANE Select NP_775099.2:p.Lys750Glu
NR_103740.2:n.2690A>G
NM_015657.4:c.1294A>G NP_056472.2:p.Lys432Glu