Canonical Allele Identifier: CA697263957

Gene: ALOX5AP

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30758410A>T , CM000675.2:g.30758410A>T	GRCh38
NC_000013.10:g.31332547A>T , CM000675.1:g.31332547A>T	GRCh37
NC_000013.9:g.30230547A>T	NCBI36
NG_011963.2:g.49933A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380490.5:c.323+2385A>T MANE Select	ENSP00000369858.3:n.323+2385A>T
ENST00000380490.4:c.323+2385A>T	ENSP00000369858.3:n.323+2385A>T
ENST00000617770.4:c.494+2385A>T	ENSP00000479870.1:n.494+2385A>T
NM_001204406.1:c.494+2385A>T	NP_001191335.1:n.494+2385A>T
NM_001629.3:c.323+2385A>T	NP_001620.2:n.323+2385A>T
XM_011535025.1:c.203+2385A>T	XP_011533327.1:n.203+2385A>T
XM_017020522.2:c.203+2385A>T	XP_016876011.1:n.203+2385A>T
NM_001204406.2:c.494+2385A>T	NP_001191335.1:n.494+2385A>T
NM_001629.4:c.323+2385A>T MANE Select	NP_001620.2:n.323+2385A>T