Canonical Allele Identifier: CA2326053487

Gene: JAK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17834801C= , CM000681.2:g.17834801C=	GRCh38
NC_000019.9:g.17945610C= , CM000681.1:g.17945610C=	GRCh37
NC_000019.8:g.17806610C=	NCBI36
NG_007273.1:g.18191G= , LRG_77:g.18191G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*756+51G=	ENSP00000513006.1:n.*756+51G=
ENST00000696967.1:n.1376+51G=
ENST00000696970.1:n.854+51G=
ENST00000458235.7:c.2199+51G= MANE Select	ENSP00000391676.1:n.2199+51G=
ENST00000458235.5:c.2199+51G=	ENSP00000391676.1:n.2199+51G=
ENST00000527031.5:n.2278+1926G=
ENST00000527670.5:c.2199+51G=	ENSP00000432511.1:n.2199+51G=
ENST00000534444.1:c.2199+51G=	ENSP00000436421.1:n.2199+51G=
NM_000215.3:c.2199+51G= , LRG_77t1:c.2199+51G=	NP_000206.2:n.2199+51G=
XM_005259896.2:c.2328+51G=	XP_005259953.1:n.2328+51G=
XM_006722745.2:c.2199+51G=	XP_006722808.1:n.2199+51G=
XM_011527990.1:c.2328+51G=	XP_011526292.1:n.2328+51G=
XR_430137.2:n.2338+51G=
XM_005259896.3:c.2328+51G=	XP_005259953.1:n.2328+51G=
NM_000215.4:c.2199+51G= MANE Select	NP_000206.2:n.2199+51G=