Canonical Allele Identifier: CA2673909465
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875425_56875430dup , CM000667.2:g.56875425_56875430dup GRCh38
NC_000005.9:g.56171252_56171257dup , CM000667.1:g.56171252_56171257dup GRCh37
NC_000005.8:g.56207009_56207014dup NCBI36
NG_031884.1:g.65353_65358dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.1965+115_1965+120dup MANE Select ENSP00000382423.3:n.1965+115_1965+120dup
ENST00000399503.3:c.1965+115_1965+120dup ENSP00000382423.3:n.1965+115_1965+120dup
NM_005921.1:c.1965+115_1965+120dup NP_005912.1:n.1965+115_1965+120dup
XM_005248519.3:c.1587+115_1587+120dup XP_005248576.2:n.1587+115_1587+120dup
XM_011543406.1:c.1710+115_1710+120dup XP_011541708.1:n.1710+115_1710+120dup
XM_011543407.1:c.1686+2420_1686+2425dup XP_011541709.1:n.1686+2420_1686+2425dup
XM_011543408.1:c.1965+115_1965+120dup XP_011541710.1:n.1965+115_1965+120dup
XM_017009484.1:c.1554+115_1554+120dup XP_016864973.1:n.1554+115_1554+120dup
XM_017009485.1:c.1476+115_1476+120dup XP_016864974.1:n.1476+115_1476+120dup
XR_001742068.2:n.1996+115_1996+120dup
NM_005921.2:c.1965+115_1965+120dup MANE Select NP_005912.1:n.1965+115_1965+120dup