Canonical Allele Identifier: CA306141728

Gene: JAK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17843778G>T , CM000681.2:g.17843778G>T	GRCh38
NC_000019.9:g.17954587G>T , CM000681.1:g.17954587G>T	GRCh37
NC_000019.8:g.17815587G>T	NCBI36
NG_007273.1:g.9214C>A , LRG_77:g.9214C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000215.4:c.307C>A MANE Select	NP_000206.2:p.Arg103Ser
ENST00000458235.7:c.307C>A MANE Select	ENSP00000391676.1:p.Arg103Ser
NM_000215.3:c.307C>A , LRG_77t1:c.307C>A	NP_000206.2:p.Arg103Ser
ENST00000458235.5:c.307C>A	ENSP00000391676.1:p.Arg103Ser
ENST00000526008.5:n.407C>A
ENST00000526008.6:c.307C>A	ENSP00000513006.1:p.Arg103Ser
ENST00000527031.5:n.397C>A
ENST00000527670.5:c.307C>A	ENSP00000432511.1:p.Arg103Ser
ENST00000528293.1:n.324-287C>A
ENST00000534444.1:c.307C>A	ENSP00000436421.1:p.Arg103Ser
XM_005259896.2:c.436C>A	XP_005259953.1:p.Arg146Ser
XM_005259896.3:c.436C>A	XP_005259953.1:p.Arg146Ser
XM_006722745.2:c.307C>A	XP_006722808.1:p.Arg103Ser
XM_011527990.1:c.436C>A	XP_011526292.1:p.Arg146Ser
XM_011527991.1:c.436C>A	XP_011526293.1:p.Arg146Ser
XM_011527991.2:c.436C>A	XP_011526293.1:p.Arg146Ser
XR_430137.2:n.446C>A