Canonical Allele Identifier: CA2326054508
Community Standard Title: NM_000215.4(JAK3):c.1767C= (p.Gly589=)
Gene: JAK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17837148G= , CM000681.2:g.17837148G= GRCh38
NC_000019.9:g.17947957G= , CM000681.1:g.17947957G= GRCh37
NC_000019.8:g.17808957G= NCBI36
NG_007273.1:g.15844C= , LRG_77:g.15844C=

Transcript Alleles

HGVS Amino-acid Change
NM_000215.4:c.1767C= MANE Select NP_000206.2:p.Gly589=
ENST00000458235.7:c.1767C= MANE Select ENSP00000391676.1:p.Gly589=
NM_000215.3:c.1767C= , LRG_77t1:c.1767C= NP_000206.2:p.Gly589=
ENST00000458235.5:c.1767C= ENSP00000391676.1:p.Gly589=
ENST00000526008.6:c.*324C= ENSP00000513006.1:n.*324C=
ENST00000527031.5:n.1857C=
ENST00000527670.5:c.1767C= ENSP00000432511.1:p.Gly589=
ENST00000534444.1:c.1767C= ENSP00000436421.1:p.Gly589=
ENST00000696967.1:n.944C=
ENST00000696970.1:n.422C=
XM_005259896.2:c.1896C= XP_005259953.1:p.Gly632=
XM_005259896.3:c.1896C= XP_005259953.1:p.Gly632=
XM_006722745.2:c.1767C= XP_006722808.1:p.Gly589=
XM_011527990.1:c.1896C= XP_011526292.1:p.Gly632=
XM_011527991.1:c.1896C= XP_011526293.1:p.Gly632=
XM_011527991.2:c.1896C= XP_011526293.1:p.Gly632=
XR_430137.2:n.1906C=