Canonical Allele Identifier: CA127250312

Gene: IL13

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132658770C>A , CM000667.2:g.132658770C>A	GRCh38
NC_000005.9:g.131994462C>A , CM000667.1:g.131994462C>A	GRCh37
NC_000005.8:g.132022361C>A	NCBI36
NG_012090.1:g.5598C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.174+410C>A MANE Select	ENSP00000304915.3:n.174+410C>A
ENST00000459878.5:n.178+410C>A
ENST00000462480.1:n.598C>A
ENST00000468334.5:n.548-648C>A
ENST00000487267.5:n.345+410C>A
ENST00000617259.2:c.132+410C>A	ENSP00000479835.1:n.132+410C>A
NM_002188.2:c.174+410C>A	NP_002179.2:n.174+410C>A
NM_001354991.1:c.-22+410C>A	NP_001341920.1:n.-22+410C>A
NM_001354992.1:c.-22+410C>A	NP_001341921.1:n.-22+410C>A
NM_001354993.1:c.-21-648C>A	NP_001341922.1:n.-21-648C>A
NM_002188.3:c.174+410C>A MANE Select	NP_002179.2:n.174+410C>A
NM_001354991.2:c.-22+410C>A	NP_001341920.1:n.-22+410C>A
NM_001354992.2:c.-22+410C>A	NP_001341921.1:n.-22+410C>A
NM_001354993.2:c.-21-648C>A	NP_001341922.1:n.-21-648C>A