Canonical Allele Identifier: CA350483395
Gene: ABCA12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215011446T>C , CM000664.2:g.215011446T>C GRCh38
NC_000002.11:g.215876170T>C , CM000664.1:g.215876170T>C GRCh37
NC_000002.10:g.215584415T>C NCBI36
NG_007074.1:g.131982A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.2325A>G MANE Select ENSP00000272895.7:p.Ile775Met
ENST00000272895.11:c.2325A>G ENSP00000272895.7:p.Ile775Met
ENST00000389661.4:c.1371A>G ENSP00000374312.4:p.Ile457Met
NM_015657.3:c.1371A>G NP_056472.2:p.Ile457Met
NM_173076.2:c.2325A>G NP_775099.2:p.Ile775Met
NR_103740.1:n.2569A>G
XM_011510951.1:c.2325A>G XP_011509253.1:p.Ile775Met
XM_011510952.1:c.2325A>G XP_011509254.1:p.Ile775Met
XM_011510951.2:c.2325A>G XP_011509253.1:p.Ile775Met
NM_173076.3:c.2325A>G MANE Select NP_775099.2:p.Ile775Met
NR_103740.2:n.2767A>G
NM_015657.4:c.1371A>G NP_056472.2:p.Ile457Met