Canonical Allele Identifier: CA2326057787

Gene: JAK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17843791C= , CM000681.2:g.17843791C=	GRCh38
NC_000019.9:g.17954600C= , CM000681.1:g.17954600C=	GRCh37
NC_000019.8:g.17815600C=	NCBI36
NG_007273.1:g.9201G= , LRG_77:g.9201G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.294G=	ENSP00000513006.1:p.Leu98=
ENST00000458235.7:c.294G= MANE Select	ENSP00000391676.1:p.Leu98=
ENST00000458235.5:c.294G=	ENSP00000391676.1:p.Leu98=
ENST00000526008.5:n.394G=
ENST00000527031.5:n.384G=
ENST00000527670.5:c.294G=	ENSP00000432511.1:p.Leu98=
ENST00000528293.1:n.324-300G=
ENST00000534444.1:c.294G=	ENSP00000436421.1:p.Leu98=
NM_000215.3:c.294G= , LRG_77t1:c.294G=	NP_000206.2:p.Leu98=
XM_005259896.2:c.423G=	XP_005259953.1:p.Leu141=
XM_006722745.2:c.294G=	XP_006722808.1:p.Leu98=
XM_011527990.1:c.423G=	XP_011526292.1:p.Leu141=
XM_011527991.1:c.423G=	XP_011526293.1:p.Leu141=
XR_430137.2:n.433G=
XM_005259896.3:c.423G=	XP_005259953.1:p.Leu141=
XM_011527991.2:c.423G=	XP_011526293.1:p.Leu141=
NM_000215.4:c.294G= MANE Select	NP_000206.2:p.Leu98=