Canonical Allele Identifier: CA2326056508

Gene: JAK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17841711G= , CM000681.2:g.17841711G=	GRCh38
NC_000019.9:g.17952520G= , CM000681.1:g.17952520G=	GRCh37
NC_000019.8:g.17813520G=	NCBI36
NG_007273.1:g.11281C= , LRG_77:g.11281C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000215.4:c.913C= MANE Select	NP_000206.2:p.Gln305=
ENST00000458235.7:c.913C= MANE Select	ENSP00000391676.1:p.Gln305=
NM_000215.3:c.913C= , LRG_77t1:c.913C=	NP_000206.2:p.Gln305=
ENST00000458235.5:c.913C=	ENSP00000391676.1:p.Gln305=
ENST00000526008.5:n.1013C=
ENST00000526008.6:c.913C=	ENSP00000513006.1:p.Gln305=
ENST00000527031.5:n.1003C=
ENST00000527670.5:c.913C=	ENSP00000432511.1:p.Gln305=
ENST00000528705.1:n.262C=
ENST00000534444.1:c.913C=	ENSP00000436421.1:p.Gln305=
ENST00000696967.1:n.90C=
XM_005259896.2:c.1042C=	XP_005259953.1:p.Gln348=
XM_005259896.3:c.1042C=	XP_005259953.1:p.Gln348=
XM_006722745.2:c.913C=	XP_006722808.1:p.Gln305=
XM_011527990.1:c.1042C=	XP_011526292.1:p.Gln348=
XM_011527991.1:c.1042C=	XP_011526293.1:p.Gln348=
XM_011527991.2:c.1042C=	XP_011526293.1:p.Gln348=
XR_430137.2:n.1052C=