Canonical Allele Identifier: CA2326051178

Gene: JAK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17829955A= , CM000681.2:g.17829955A=	GRCh38
NC_000019.9:g.17940764A= , CM000681.1:g.17940764A=	GRCh37
NC_000019.8:g.17801764A=	NCBI36
NG_007273.1:g.23037T= , LRG_77:g.23037T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*1764+153T=	ENSP00000513006.1:n.*1764+153T=
ENST00000696967.1:n.2384+153T=
ENST00000696968.1:n.440+153T=
ENST00000696969.1:n.2164+153T=
ENST00000458235.7:c.3207+153T= MANE Select	ENSP00000391676.1:n.3207+153T=
ENST00000458235.5:c.3207+153T=	ENSP00000391676.1:n.3207+153T=
ENST00000527031.5:n.2279-4645T=
ENST00000527670.5:c.3207+153T=	ENSP00000432511.1:n.3207+153T=
ENST00000534444.1:c.*75T=	ENSP00000436421.1:n.*75T=
NM_000215.3:c.3207+153T= , LRG_77t1:c.3207+153T=	NP_000206.2:n.3207+153T=
XM_005259896.2:c.3336+153T=	XP_005259953.1:n.3336+153T=
XM_006722745.2:c.3207+153T=	XP_006722808.1:n.3207+153T=
XM_005259896.3:c.3336+153T=	XP_005259953.1:n.3336+153T=
NM_000215.4:c.3207+153T= MANE Select	NP_000206.2:n.3207+153T=