Canonical Allele Identifier: CA404767974

Gene: JAK3

Linked Data

• COSMIC: COSM6191556
• MyVariant Identifiers: chr19:g.17945790C>T (hg19) ; chr19:g.17834981C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17834981C>T , CM000681.2:g.17834981C>T	GRCh38
NC_000019.9:g.17945790C>T , CM000681.1:g.17945790C>T	GRCh37
NC_000019.8:g.17806790C>T	NCBI36
NG_007273.1:g.18011G>A , LRG_77:g.18011G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*627G>A	ENSP00000513006.1:n.*627G>A
ENST00000696967.1:n.1247G>A
ENST00000696970.1:n.725G>A
ENST00000458235.7:c.2070G>A MANE Select	ENSP00000391676.1:p.Trp690Ter
ENST00000458235.5:c.2070G>A	ENSP00000391676.1:p.Trp690Ter
ENST00000527031.5:n.2278+1746G>A
ENST00000527670.5:c.2070G>A	ENSP00000432511.1:p.Trp690Ter
ENST00000534444.1:c.2070G>A	ENSP00000436421.1:p.Trp690Ter
NM_000215.3:c.2070G>A , LRG_77t1:c.2070G>A	NP_000206.2:p.Trp690Ter
XM_005259896.2:c.2199G>A	XP_005259953.1:p.Trp733Ter
XM_006722745.2:c.2070G>A	XP_006722808.1:p.Trp690Ter
XM_011527990.1:c.2199G>A	XP_011526292.1:p.Trp733Ter
XR_430137.2:n.2209G>A
XM_005259896.3:c.2199G>A	XP_005259953.1:p.Trp733Ter
NM_000215.4:c.2070G>A MANE Select	NP_000206.2:p.Trp690Ter