Canonical Allele Identifier: CA697266602

Gene: ALOX5AP

Linked Data

• dbSNP Id: rs1434094556
• gnomAD v3: 13-30763773-T-C
• gnomAD v4: 13-30763773-T-C
• MyVariant Identifiers: chr13:g.31337910T>C (hg19) ; chr13:g.30763773T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30763773T>C , CM000675.2:g.30763773T>C	GRCh38
NC_000013.10:g.31337910T>C , CM000675.1:g.31337910T>C	GRCh37
NC_000013.9:g.30235910T>C	NCBI36
NG_011963.2:g.55296T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380490.5:c.324-171T>C MANE Select	ENSP00000369858.3:n.324-171T>C
ENST00000380490.4:c.324-171T>C	ENSP00000369858.3:n.324-171T>C
ENST00000617770.4:c.495-171T>C	ENSP00000479870.1:n.495-171T>C
NM_001204406.1:c.495-171T>C	NP_001191335.1:n.495-171T>C
NM_001629.3:c.324-171T>C	NP_001620.2:n.324-171T>C
XM_011535025.1:c.204-171T>C	XP_011533327.1:n.204-171T>C
XM_017020522.2:c.204-171T>C	XP_016876011.1:n.204-171T>C
NM_001204406.2:c.495-171T>C	NP_001191335.1:n.495-171T>C
NM_001629.4:c.324-171T>C MANE Select	NP_001620.2:n.324-171T>C