Canonical Allele Identifier: CA2326057623
Gene: JAK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17843353T= , CM000681.2:g.17843353T= GRCh38
NC_000019.9:g.17954162T= , CM000681.1:g.17954162T= GRCh37
NC_000019.8:g.17815162T= NCBI36
NG_007273.1:g.9639A= , LRG_77:g.9639A=

Transcript Alleles

HGVS Amino-acid change
ENST00000526008.6:c.420+27A= ENSP00000513006.1:n.420+27A=
ENST00000458235.7:c.420+27A= MANE Select ENSP00000391676.1:n.420+27A=
ENST00000458235.5:c.420+27A= ENSP00000391676.1:n.420+27A=
ENST00000526008.5:n.520+27A=
ENST00000527031.5:n.510+27A=
ENST00000527670.5:c.420+27A= ENSP00000432511.1:n.420+27A=
ENST00000528293.1:n.435+27A=
ENST00000534444.1:c.420+27A= ENSP00000436421.1:n.420+27A=
NM_000215.3:c.420+27A= , LRG_77t1:c.420+27A= NP_000206.2:n.420+27A=
XM_005259896.2:c.549+27A= XP_005259953.1:n.549+27A=
XM_006722745.2:c.420+27A= XP_006722808.1:n.420+27A=
XM_011527990.1:c.549+27A= XP_011526292.1:n.549+27A=
XM_011527991.1:c.549+27A= XP_011526293.1:n.549+27A=
XR_430137.2:n.559+27A=
XM_005259896.3:c.549+27A= XP_005259953.1:n.549+27A=
XM_011527991.2:c.549+27A= XP_011526293.1:n.549+27A=
NM_000215.4:c.420+27A= MANE Select NP_000206.2:n.420+27A=