Canonical Allele Identifier: CA1583277042

Gene: IL4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132682440A= , CM000667.2:g.132682440A=	GRCh38
NC_000005.9:g.132018132A= , CM000667.1:g.132018132A=	GRCh37
NC_000005.8:g.132046031A=	NCBI36
NG_023252.1:g.13760A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231449.7:c.361-46A= MANE Select	ENSP00000231449.2:n.361-46A=
ENST00000231449.6:c.361-46A=	ENSP00000231449.2:n.361-46A=
ENST00000350025.2:c.313-46A=	ENSP00000325190.3:n.313-46A=
ENST00000622422.1:c.*51-46A=	ENSP00000480581.1:n.*51-46A=
NM_000589.3:c.361-46A=	NP_000580.1:n.361-46A=
NM_172348.2:c.313-46A=	NP_758858.1:n.313-46A=
XR_948791.1:n.176+14T=
NM_001354990.1:c.*51-46A=	NP_001341919.1:n.*51-46A=
NR_134248.1:n.176+14T=
NM_000589.4:c.361-46A= MANE Select	NP_000580.1:n.361-46A=
NM_172348.3:c.313-46A=	NP_758858.1:n.313-46A=
NM_001354990.2:c.*51-46A=	NP_001341919.1:n.*51-46A=