Canonical Allele Identifier: CA2646050493

Linked Data

gnomAD v4: 1-64833252-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.64833252G>T , CM000663.2:g.64833252G>T GRCh38
NC_000001.10:g.65298935G>T , CM000663.1:g.65298935G>T GRCh37
NC_000001.9:g.65071523G>T NCBI36
NG_023402.1:g.138253C>A
NG_023402.2:g.239495C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465376.7:n.3115C>A (JAK1)
ENST00000671746.2:c.*4683C>A (JAK1) ENSP00000500065.1:n.*4683C>A
ENST00000671929.2:c.*1310C>A (JAK1) ENSP00000500485.1:n.*1310C>A
ENST00000671954.2:c.*1310C>A (JAK1) ENSP00000500841.1:n.*1310C>A
ENST00000672179.2:c.*1310C>A (JAK1) ENSP00000500296.1:n.*1310C>A
ENST00000672247.2:c.*1310C>A (JAK1) ENSP00000499884.1:n.*1310C>A
ENST00000672434.2:c.*1310C>A (JAK1) ENSP00000499900.1:n.*1310C>A
ENST00000672574.2:c.*1310C>A (JAK1) ENSP00000500714.2:n.*1310C>A
ENST00000672751.2:c.*1310C>A (JAK1) ENSP00000500745.2:n.*1310C>A
ENST00000673246.2:c.*1310C>A (JAK1) ENSP00000499942.2:n.*1310C>A
ENST00000673314.2:n.6074C>A (JAK1)
ENST00000673502.2:n.6234C>A (JAK1)
ENST00000699259.1:c.*1310C>A (JAK1) ENSP00000514240.1:n.*1310C>A
ENST00000699260.1:c.*1310C>A (JAK1) ENSP00000514241.1:n.*1310C>A
ENST00000699261.1:c.*2149C>A (JAK1) ENSP00000514242.1:n.*2149C>A
ENST00000699310.1:c.*1310C>A (JAK1) ENSP00000514289.1:n.*1310C>A
ENST00000699311.1:c.*3435C>A (JAK1) ENSP00000514290.1:n.*3435C>A
ENST00000699312.1:c.*1310C>A (JAK1) ENSP00000514291.1:n.*1310C>A
ENST00000699313.1:c.*3284C>A (JAK1) ENSP00000514292.1:n.*3284C>A
ENST00000342505.5:c.*1310C>A (JAK1) MANE Select ENSP00000343204.4:n.*1310C>A
ENST00000671746.1:c.*4683C>A (JAK1) ENSP00000500065.1:n.*4683C>A
ENST00000672247.1:c.*1310C>A (JAK1) ENSP00000499884.1:n.*1310C>A
ENST00000672434.1:c.*1310C>A (JAK1) ENSP00000499900.1:n.*1310C>A
ENST00000672574.1:c.2716C>A (JAK1)
ENST00000673046.1:c.*1310C>A (JAK1) ENSP00000500878.1:n.*1310C>A
ENST00000342505.4:c.*1310C>A (JAK1) ENSP00000343204.4:n.*1310C>A
NM_002227.2:c.*1310C>A (JAK1) NP_002218.2:n.*1310C>A
XM_005270841.1:c.*1310C>A (JAK1) XP_005270898.1:n.*1310C>A
XM_006710624.1:c.*1310C>A (JAK1) XP_006710687.1:n.*1310C>A
XM_011541395.1:c.*1310C>A (JAK1) XP_011539697.1:n.*1310C>A
NM_001320923.1:c.*1310C>A (JAK1) NP_001307852.1:n.*1310C>A
NM_001321852.1:c.*1310C>A (JAK1) NP_001308781.1:n.*1310C>A
NM_001321853.1:c.*1310C>A (JAK1) NP_001308782.1:n.*1310C>A
NM_001321854.1:c.*1310C>A (JAK1) NP_001308783.1:n.*1310C>A
NM_001321855.1:c.*1310C>A (JAK1) NP_001308784.1:n.*1310C>A
NM_001321856.1:c.*1310C>A (JAK1) NP_001308785.1:n.*1310C>A
NM_001321857.1:c.*1310C>A (JAK1) NP_001308786.1:n.*1310C>A
NM_002227.3:c.*1310C>A (JAK1) NP_002218.2:n.*1310C>A
XR_946693.3:n.4686G>T (RAVER2)
NM_002227.4:c.*1310C>A (JAK1) MANE Select NP_002218.2:n.*1310C>A
NM_001321852.2:c.*1310C>A (JAK1) NP_001308781.1:n.*1310C>A
NM_001321853.2:c.*1310C>A (JAK1) NP_001308782.1:n.*1310C>A
NM_001321854.2:c.*1310C>A (JAK1) NP_001308783.1:n.*1310C>A
NM_001321855.2:c.*1310C>A (JAK1) NP_001308784.1:n.*1310C>A
NM_001321857.2:c.*1310C>A (JAK1) NP_001308786.1:n.*1310C>A
NM_001320923.2:c.*1310C>A (JAK1) NP_001307852.1:n.*1310C>A
NM_001321856.2:c.*1310C>A (JAK1) NP_001308785.1:n.*1310C>A