Canonical Allele Identifier: CA2326053600

Gene: JAK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17835048C= , CM000681.2:g.17835048C=	GRCh38
NC_000019.9:g.17945857C= , CM000681.1:g.17945857C=	GRCh37
NC_000019.8:g.17806857C=	NCBI36
NG_007273.1:g.17944G= , LRG_77:g.17944G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*604+35G=	ENSP00000513006.1:n.*604+35G=
ENST00000696967.1:n.1224+35G=
ENST00000696970.1:n.702+35G=
ENST00000458235.7:c.2047+35G= MANE Select	ENSP00000391676.1:n.2047+35G=
ENST00000458235.5:c.2047+35G=	ENSP00000391676.1:n.2047+35G=
ENST00000527031.5:n.2278+1679G=
ENST00000527670.5:c.2047+35G=	ENSP00000432511.1:n.2047+35G=
ENST00000534444.1:c.2047+35G=	ENSP00000436421.1:n.2047+35G=
NM_000215.3:c.2047+35G= , LRG_77t1:c.2047+35G=	NP_000206.2:n.2047+35G=
XM_005259896.2:c.2176+35G=	XP_005259953.1:n.2176+35G=
XM_006722745.2:c.2047+35G=	XP_006722808.1:n.2047+35G=
XM_011527990.1:c.2176+35G=	XP_011526292.1:n.2176+35G=
XR_430137.2:n.2186+35G=
XM_005259896.3:c.2176+35G=	XP_005259953.1:n.2176+35G=
NM_000215.4:c.2047+35G= MANE Select	NP_000206.2:n.2047+35G=