Canonical Allele Identifier: CA1172054148
Gene: JAK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.64833570G= , CM000663.2:g.64833570G= GRCh38
NC_000001.10:g.65299253G= , CM000663.1:g.65299253G= GRCh37
NC_000001.9:g.65071841G= NCBI36
NG_023402.1:g.137935C=
NG_023402.2:g.239177C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465376.7:n.2797C=
ENST00000671746.2:c.*4365C= ENSP00000500065.1:n.*4365C=
ENST00000671929.2:c.*992C= ENSP00000500485.1:n.*992C=
ENST00000671954.2:c.*992C= ENSP00000500841.1:n.*992C=
ENST00000672179.2:c.*992C= ENSP00000500296.1:n.*992C=
ENST00000672247.2:c.*992C= ENSP00000499884.1:n.*992C=
ENST00000672434.2:c.*992C= ENSP00000499900.1:n.*992C=
ENST00000672574.2:c.*992C= ENSP00000500714.2:n.*992C=
ENST00000672751.2:c.*992C= ENSP00000500745.2:n.*992C=
ENST00000673246.2:c.*992C= ENSP00000499942.2:n.*992C=
ENST00000673314.2:n.5756C=
ENST00000673502.2:n.5916C=
ENST00000699259.1:c.*992C= ENSP00000514240.1:n.*992C=
ENST00000699260.1:c.*992C= ENSP00000514241.1:n.*992C=
ENST00000699261.1:c.*1831C= ENSP00000514242.1:n.*1831C=
ENST00000699310.1:c.*992C= ENSP00000514289.1:n.*992C=
ENST00000699311.1:c.*3117C= ENSP00000514290.1:n.*3117C=
ENST00000699312.1:c.*992C= ENSP00000514291.1:n.*992C=
ENST00000699313.1:c.*2966C= ENSP00000514292.1:n.*2966C=
ENST00000342505.5:c.*992C= MANE Select ENSP00000343204.4:n.*992C=
ENST00000671746.1:c.*4365C= ENSP00000500065.1:n.*4365C=
ENST00000671929.1:c.*992C= ENSP00000500485.1:n.*992C=
ENST00000671954.1:c.*992C= ENSP00000500841.1:n.*992C=
ENST00000672179.1:c.*992C= ENSP00000500296.1:n.*992C=
ENST00000672247.1:c.*992C= ENSP00000499884.1:n.*992C=
ENST00000672434.1:c.*992C= ENSP00000499900.1:n.*992C=
ENST00000672574.1:c.2398C=
ENST00000673046.1:c.*992C= ENSP00000500878.1:n.*992C=
ENST00000673220.1:c.*6866C= ENSP00000500422.1:n.*6866C=
ENST00000673246.1:c.3972C=
ENST00000673254.1:c.*992C= ENSP00000500476.1:n.*992C=
ENST00000673314.1:n.5553C=
ENST00000342505.4:c.*992C= ENSP00000343204.4:n.*992C=
NM_002227.2:c.*992C= NP_002218.2:n.*992C=
XM_005270841.1:c.*992C= XP_005270898.1:n.*992C=
XM_006710624.1:c.*992C= XP_006710687.1:n.*992C=
XM_011541395.1:c.*992C= XP_011539697.1:n.*992C=
NM_001320923.1:c.*992C= NP_001307852.1:n.*992C=
NM_001321852.1:c.*992C= NP_001308781.1:n.*992C=
NM_001321853.1:c.*992C= NP_001308782.1:n.*992C=
NM_001321854.1:c.*992C= NP_001308783.1:n.*992C=
NM_001321855.1:c.*992C= NP_001308784.1:n.*992C=
NM_001321856.1:c.*992C= NP_001308785.1:n.*992C=
NM_001321857.1:c.*992C= NP_001308786.1:n.*992C=
NM_002227.3:c.*992C= NP_002218.2:n.*992C=
NM_002227.4:c.*992C= MANE Select NP_002218.2:n.*992C=
NM_001321852.2:c.*992C= NP_001308781.1:n.*992C=
NM_001321853.2:c.*992C= NP_001308782.1:n.*992C=
NM_001321854.2:c.*992C= NP_001308783.1:n.*992C=
NM_001321855.2:c.*992C= NP_001308784.1:n.*992C=
NM_001321857.2:c.*992C= NP_001308786.1:n.*992C=
NM_001320923.2:c.*992C= NP_001307852.1:n.*992C=
NM_001321856.2:c.*992C= NP_001308785.1:n.*992C=