Canonical Allele Identifier: CA1139788276

Gene: JAK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.64840499C= , CM000663.2:g.64840499C=	GRCh38
NC_000001.10:g.65306182C= , CM000663.1:g.65306182C=	GRCh37
NC_000001.9:g.65078770C=	NCBI36
NG_023402.1:g.131006G=
NG_023402.2:g.232248G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465376.7:n.990-704G=
ENST00000671746.2:c.*2558-704G=	ENSP00000500065.1:n.*2558-704G=
ENST00000671929.2:c.2650-704G=	ENSP00000500485.1:n.2650-704G=
ENST00000671954.2:c.2650-704G=	ENSP00000500841.1:n.2650-704G=
ENST00000672179.2:c.2650-704G=	ENSP00000500296.1:n.2650-704G=
ENST00000672247.2:c.2650-704G=	ENSP00000499884.1:n.2650-704G=
ENST00000672434.2:c.2650-704G=	ENSP00000499900.1:n.2650-704G=
ENST00000672574.2:c.2545-704G=	ENSP00000500714.2:n.2545-704G=
ENST00000672751.2:c.2650-704G=	ENSP00000500745.2:n.2650-704G=
ENST00000673246.2:c.2521-704G=	ENSP00000499942.2:n.2521-704G=
ENST00000673314.2:n.3949-704G=
ENST00000673502.2:n.4109-704G=
ENST00000699259.1:c.2647-704G=	ENSP00000514240.1:n.2647-704G=
ENST00000699260.1:c.2647-704G=	ENSP00000514241.1:n.2647-704G=
ENST00000699261.1:c.*24-704G=	ENSP00000514242.1:n.*24-704G=
ENST00000699262.1:c.2650-704G=	ENSP00000514243.1:n.2650-704G=
ENST00000699310.1:c.2644-704G=	ENSP00000514289.1:n.2644-704G=
ENST00000699311.1:c.*1310-704G=	ENSP00000514290.1:n.*1310-704G=
ENST00000699312.1:c.2650-704G=	ENSP00000514291.1:n.2650-704G=
ENST00000699313.1:c.*1159-704G=	ENSP00000514292.1:n.*1159-704G=
ENST00000342505.5:c.2650-704G= MANE Select	ENSP00000343204.4:n.2650-704G=
ENST00000465376.6:n.951-704G=
ENST00000671746.1:c.*2558-704G=	ENSP00000500065.1:n.*2558-704G=
ENST00000671929.1:c.2650-704G=	ENSP00000500485.1:n.2650-704G=
ENST00000671954.1:c.2650-704G=	ENSP00000500841.1:n.2650-704G=
ENST00000672179.1:c.2650-704G=	ENSP00000500296.1:n.2650-704G=
ENST00000672247.1:c.2650-704G=	ENSP00000499884.1:n.2650-704G=
ENST00000672434.1:c.2650-704G=	ENSP00000499900.1:n.2650-704G=
ENST00000672574.1:c.591-704G=
ENST00000673046.1:c.2644-704G=	ENSP00000500878.1:n.2644-704G=
ENST00000673220.1:c.*5059-704G=	ENSP00000500422.1:n.*5059-704G=
ENST00000673246.1:c.2165-704G=
ENST00000673254.1:c.2518-704G=	ENSP00000500476.1:n.2518-704G=
ENST00000673314.1:n.3746-704G=
ENST00000342505.4:c.2650-704G=	ENSP00000343204.4:n.2650-704G=
ENST00000481702.1:n.15-704G=
NM_002227.2:c.2650-704G=	NP_002218.2:n.2650-704G=
XM_005270841.1:c.2650-704G=	XP_005270898.1:n.2650-704G=
XM_006710624.1:c.2650-704G=	XP_006710687.1:n.2650-704G=
XM_011541395.1:c.2647-704G=	XP_011539697.1:n.2647-704G=
NM_001320923.1:c.2650-704G=	NP_001307852.1:n.2650-704G=
NM_001321852.1:c.2650-704G=	NP_001308781.1:n.2650-704G=
NM_001321853.1:c.2650-704G=	NP_001308782.1:n.2650-704G=
NM_001321854.1:c.2650-704G=	NP_001308783.1:n.2650-704G=
NM_001321855.1:c.2650-704G=	NP_001308784.1:n.2650-704G=
NM_001321856.1:c.2650-704G=	NP_001308785.1:n.2650-704G=
NM_001321857.1:c.2647-704G=	NP_001308786.1:n.2647-704G=
NM_002227.3:c.2650-704G=	NP_002218.2:n.2650-704G=
NM_002227.4:c.2650-704G= MANE Select	NP_002218.2:n.2650-704G=
NM_001321852.2:c.2650-704G=	NP_001308781.1:n.2650-704G=
NM_001321853.2:c.2650-704G=	NP_001308782.1:n.2650-704G=
NM_001321854.2:c.2650-704G=	NP_001308783.1:n.2650-704G=
NM_001321855.2:c.2650-704G=	NP_001308784.1:n.2650-704G=
NM_001321857.2:c.2647-704G=	NP_001308786.1:n.2647-704G=
NM_001320923.2:c.2650-704G=	NP_001307852.1:n.2650-704G=
NM_001321856.2:c.2650-704G=	NP_001308785.1:n.2650-704G=