Canonical Allele Identifier: CA2326054888
Gene: JAK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17837938G= , CM000681.2:g.17837938G= GRCh38
NC_000019.9:g.17948747G= , CM000681.1:g.17948747G= GRCh37
NC_000019.8:g.17809747G= NCBI36
NG_007273.1:g.15054C= , LRG_77:g.15054C=

Transcript Alleles

HGVS Amino-acid Change
NM_000215.4:c.1695C= MANE Select NP_000206.2:p.Cys565=
ENST00000458235.7:c.1695C= MANE Select ENSP00000391676.1:p.Cys565=
NM_000215.3:c.1695C= , LRG_77t1:c.1695C= NP_000206.2:p.Cys565=
ENST00000458235.5:c.1695C= ENSP00000391676.1:p.Cys565=
ENST00000526008.6:c.*252C= ENSP00000513006.1:n.*252C=
ENST00000527031.5:n.1785C=
ENST00000527670.5:c.1695C= ENSP00000432511.1:p.Cys565=
ENST00000534444.1:c.1695C= ENSP00000436421.1:p.Cys565=
ENST00000696967.1:n.872C=
ENST00000696970.1:n.350C=
XM_005259896.2:c.1824C= XP_005259953.1:p.Cys608=
XM_005259896.3:c.1824C= XP_005259953.1:p.Cys608=
XM_006722745.2:c.1695C= XP_006722808.1:p.Cys565=
XM_011527990.1:c.1824C= XP_011526292.1:p.Cys608=
XM_011527991.1:c.1824C= XP_011526293.1:p.Cys608=
XM_011527991.2:c.1824C= XP_011526293.1:p.Cys608=
XR_430137.2:n.1834C=