Canonical Allele Identifier: CA1548136424
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875171G= , CM000667.2:g.56875171G= GRCh38
NC_000005.9:g.56170998G= , CM000667.1:g.56170998G= GRCh37
NC_000005.8:g.56206755G= NCBI36
NG_031884.1:g.65099G=

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.1826G= MANE Select ENSP00000382423.3:p.Ser609=
ENST00000399503.3:c.1826G= ENSP00000382423.3:p.Ser609=
NM_005921.1:c.1826G= NP_005912.1:p.Ser609=
XM_005248519.3:c.1448G= XP_005248576.2:p.Ser483=
XM_011543406.1:c.1571G= XP_011541708.1:p.Ser524=
XM_011543407.1:c.1686+2166G= XP_011541709.1:n.1686+2166G=
XM_011543408.1:c.1826G= XP_011541710.1:p.Ser609=
XM_017009484.1:c.1415G= XP_016864973.1:p.Ser472=
XM_017009485.1:c.1337G= XP_016864974.1:p.Ser446=
XR_001742068.2:n.1857G=
NM_005921.2:c.1826G= MANE Select NP_005912.1:p.Ser609=