Canonical Allele Identifier: CA2326057921

Gene: JAK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17844112T= , CM000681.2:g.17844112T=	GRCh38
NC_000019.9:g.17954921T= , CM000681.1:g.17954921T=	GRCh37
NC_000019.8:g.17815921T=	NCBI36
NG_007273.1:g.8880A= , LRG_77:g.8880A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.184+122A=	ENSP00000513006.1:n.184+122A=
ENST00000458235.7:c.184+122A= MANE Select	ENSP00000391676.1:n.184+122A=
ENST00000458235.5:c.184+122A=	ENSP00000391676.1:n.184+122A=
ENST00000526008.5:n.284+122A=
ENST00000527031.5:n.274+122A=
ENST00000527670.5:c.184+122A=	ENSP00000432511.1:n.184+122A=
ENST00000528293.1:n.323+122A=
ENST00000534444.1:c.184+122A=	ENSP00000436421.1:n.184+122A=
NM_000215.3:c.184+122A= , LRG_77t1:c.184+122A=	NP_000206.2:n.184+122A=
XM_005259896.2:c.313+122A=	XP_005259953.1:n.313+122A=
XM_006722745.2:c.184+122A=	XP_006722808.1:n.184+122A=
XM_011527990.1:c.313+122A=	XP_011526292.1:n.313+122A=
XM_011527991.1:c.313+122A=	XP_011526293.1:n.313+122A=
XR_430137.2:n.323+122A=
XM_005259896.3:c.313+122A=	XP_005259953.1:n.313+122A=
XM_011527991.2:c.313+122A=	XP_011526293.1:n.313+122A=
NM_000215.4:c.184+122A= MANE Select	NP_000206.2:n.184+122A=