Canonical Allele Identifier: CA2326057501

Gene: JAK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17843115C= , CM000681.2:g.17843115C=	GRCh38
NC_000019.9:g.17953924C= , CM000681.1:g.17953924C=	GRCh37
NC_000019.8:g.17814924C=	NCBI36
NG_007273.1:g.9877G= , LRG_77:g.9877G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.478G=	ENSP00000513006.1:p.Gly160=
ENST00000458235.7:c.478G= MANE Select	ENSP00000391676.1:p.Gly160=
ENST00000458235.5:c.478G=	ENSP00000391676.1:p.Gly160=
ENST00000526008.5:n.578G=
ENST00000527031.5:n.568G=
ENST00000527670.5:c.478G=	ENSP00000432511.1:p.Gly160=
ENST00000528293.1:n.493G=
ENST00000534444.1:c.478G=	ENSP00000436421.1:p.Gly160=
NM_000215.3:c.478G= , LRG_77t1:c.478G=	NP_000206.2:p.Gly160=
XM_005259896.2:c.607G=	XP_005259953.1:p.Gly203=
XM_006722745.2:c.478G=	XP_006722808.1:p.Gly160=
XM_011527990.1:c.607G=	XP_011526292.1:p.Gly203=
XM_011527991.1:c.607G=	XP_011526293.1:p.Gly203=
XR_430137.2:n.617G=
XM_005259896.3:c.607G=	XP_005259953.1:p.Gly203=
XM_011527991.2:c.607G=	XP_011526293.1:p.Gly203=
NM_000215.4:c.478G= MANE Select	NP_000206.2:p.Gly160=