Canonical Allele Identifier: CA1548139274
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881725G= , CM000667.2:g.56881725G= GRCh38
NC_000005.9:g.56177552G= , CM000667.1:g.56177552G= GRCh37
NC_000005.8:g.56213309G= NCBI36
NG_031884.1:g.71653G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2525G= MANE Select ENSP00000382423.3:p.Ser842=
ENST00000399503.3:c.2525G= ENSP00000382423.3:p.Ser842=
NM_005921.1:c.2525G= NP_005912.1:p.Ser842=
XM_005248519.3:c.2147G= XP_005248576.2:p.Ser716=
XM_011543406.1:c.2270G= XP_011541708.1:p.Ser757=
XM_011543407.1:c.2246G= XP_011541709.1:p.Ser749=
XM_011543408.1:c.2525G= XP_011541710.1:p.Ser842=
XM_017009484.1:c.2114G= XP_016864973.1:p.Ser705=
XM_017009485.1:c.2036G= XP_016864974.1:p.Ser679=
XR_001742068.2:n.2556G=
NM_005921.2:c.2525G= MANE Select NP_005912.1:p.Ser842=