Canonical Allele Identifier: CA404773526
Gene: JAK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17843390A>G , CM000681.2:g.17843390A>G GRCh38
NC_000019.9:g.17954199A>G , CM000681.1:g.17954199A>G GRCh37
NC_000019.8:g.17815199A>G NCBI36
NG_007273.1:g.9602T>C , LRG_77:g.9602T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.410T>C ENSP00000513006.1:p.Leu137Pro
ENST00000458235.7:c.410T>C MANE Select ENSP00000391676.1:p.Leu137Pro
ENST00000458235.5:c.410T>C ENSP00000391676.1:p.Leu137Pro
ENST00000526008.5:n.510T>C
ENST00000527031.5:n.500T>C
ENST00000527670.5:c.410T>C ENSP00000432511.1:p.Leu137Pro
ENST00000528293.1:n.425T>C
ENST00000534444.1:c.410T>C ENSP00000436421.1:p.Leu137Pro
NM_000215.3:c.410T>C , LRG_77t1:c.410T>C NP_000206.2:p.Leu137Pro
XM_005259896.2:c.539T>C XP_005259953.1:p.Leu180Pro
XM_006722745.2:c.410T>C XP_006722808.1:p.Leu137Pro
XM_011527990.1:c.539T>C XP_011526292.1:p.Leu180Pro
XM_011527991.1:c.539T>C XP_011526293.1:p.Leu180Pro
XR_430137.2:n.549T>C
XM_005259896.3:c.539T>C XP_005259953.1:p.Leu180Pro
XM_011527991.2:c.539T>C XP_011526293.1:p.Leu180Pro
NM_000215.4:c.410T>C MANE Select NP_000206.2:p.Leu137Pro