Canonical Allele Identifier: CA13808307
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs4769873

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30738552C>T , CM000675.2:g.30738552C>T GRCh38
NC_000013.10:g.31312689C>T , CM000675.1:g.31312689C>T GRCh37
NC_000013.9:g.30210689C>T NCBI36
NG_011963.2:g.30075C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000380490.5:c.70+2877C>T MANE Select ENSP00000369858.3:n.70+2877C>T
ENST00000380490.4:c.70+2877C>T ENSP00000369858.3:n.70+2877C>T
ENST00000617770.4:c.241+2877C>T ENSP00000479870.1:n.241+2877C>T
NM_001204406.1:c.241+2877C>T NP_001191335.1:n.241+2877C>T
NM_001629.3:c.70+2877C>T NP_001620.2:n.70+2877C>T
XM_011535024.1:c.70+2877C>T XP_011533326.1:n.70+2877C>T
NM_001204406.2:c.241+2877C>T NP_001191335.1:n.241+2877C>T
NM_001629.4:c.70+2877C>T MANE Select NP_001620.2:n.70+2877C>T