Canonical Allele Identifier: CA1548136532
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875456T= , CM000667.2:g.56875456T= GRCh38
NC_000005.9:g.56171283T= , CM000667.1:g.56171283T= GRCh37
NC_000005.8:g.56207040T= NCBI36
NG_031884.1:g.65384T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.1965+146T= MANE Select ENSP00000382423.3:n.1965+146T=
ENST00000399503.3:c.1965+146T= ENSP00000382423.3:n.1965+146T=
NM_005921.1:c.1965+146T= NP_005912.1:n.1965+146T=
XM_005248519.3:c.1587+146T= XP_005248576.2:n.1587+146T=
XM_011543406.1:c.1710+146T= XP_011541708.1:n.1710+146T=
XM_011543407.1:c.1686+2451T= XP_011541709.1:n.1686+2451T=
XM_011543408.1:c.1965+146T= XP_011541710.1:n.1965+146T=
XM_017009484.1:c.1554+146T= XP_016864973.1:n.1554+146T=
XM_017009485.1:c.1476+146T= XP_016864974.1:n.1476+146T=
XR_001742068.2:n.1996+146T=
NM_005921.2:c.1965+146T= MANE Select NP_005912.1:n.1965+146T=