Canonical Allele Identifier: CA649892017
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875454A>G , CM000667.2:g.56875454A>G GRCh38
NC_000005.9:g.56171281A>G , CM000667.1:g.56171281A>G GRCh37
NC_000005.8:g.56207038A>G NCBI36
NG_031884.1:g.65382A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.1965+144A>G MANE Select ENSP00000382423.3:n.1965+144A>G
ENST00000399503.3:c.1965+144A>G ENSP00000382423.3:n.1965+144A>G
NM_005921.1:c.1965+144A>G NP_005912.1:n.1965+144A>G
XM_005248519.3:c.1587+144A>G XP_005248576.2:n.1587+144A>G
XM_011543406.1:c.1710+144A>G XP_011541708.1:n.1710+144A>G
XM_011543407.1:c.1686+2449A>G XP_011541709.1:n.1686+2449A>G
XM_011543408.1:c.1965+144A>G XP_011541710.1:n.1965+144A>G
XM_017009484.1:c.1554+144A>G XP_016864973.1:n.1554+144A>G
XM_017009485.1:c.1476+144A>G XP_016864974.1:n.1476+144A>G
XR_001742068.2:n.1996+144A>G
NM_005921.2:c.1965+144A>G MANE Select NP_005912.1:n.1965+144A>G