Canonical Allele Identifier: CA404769129

Gene: JAK3

Linked Data

• gnomAD v4: 19-17837158-A-T
• MyVariant Identifiers: chr19:g.17947967A>T (hg19) ; chr19:g.17837158A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17837158A>T , CM000681.2:g.17837158A>T	GRCh38
NC_000019.9:g.17947967A>T , CM000681.1:g.17947967A>T	GRCh37
NC_000019.8:g.17808967A>T	NCBI36
NG_007273.1:g.15834T>A , LRG_77:g.15834T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000526008.6:c.*314T>A	ENSP00000513006.1:n.*314T>A
ENST00000696967.1:n.934T>A
ENST00000696970.1:n.412T>A
ENST00000458235.7:c.1757T>A MANE Select	ENSP00000391676.1:p.Leu586Gln
ENST00000458235.5:c.1757T>A	ENSP00000391676.1:p.Leu586Gln
ENST00000527031.5:n.1847T>A
ENST00000527670.5:c.1757T>A	ENSP00000432511.1:p.Leu586Gln
ENST00000534444.1:c.1757T>A	ENSP00000436421.1:p.Leu586Gln
NM_000215.3:c.1757T>A , LRG_77t1:c.1757T>A	NP_000206.2:p.Leu586Gln
XM_005259896.2:c.1886T>A	XP_005259953.1:p.Leu629Gln
XM_006722745.2:c.1757T>A	XP_006722808.1:p.Leu586Gln
XM_011527990.1:c.1886T>A	XP_011526292.1:p.Leu629Gln
XM_011527991.1:c.1886T>A	XP_011526293.1:p.Leu629Gln
XR_430137.2:n.1896T>A
XM_005259896.3:c.1886T>A	XP_005259953.1:p.Leu629Gln
XM_011527991.2:c.1886T>A	XP_011526293.1:p.Leu629Gln
NM_000215.4:c.1757T>A MANE Select	NP_000206.2:p.Leu586Gln