Canonical Allele Identifier: CA1076343123
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs1748205244

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881509dup , CM000667.2:g.56881509dup GRCh38
NC_000005.9:g.56177336dup , CM000667.1:g.56177336dup GRCh37
NC_000005.8:g.56213093dup NCBI36
NG_031884.1:g.71437dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2370-61dup MANE Select ENSP00000382423.3:n.2370-61dup
ENST00000399503.3:c.2370-61dup ENSP00000382423.3:n.2370-61dup
NM_005921.1:c.2370-61dup NP_005912.1:n.2370-61dup
XM_005248519.3:c.1992-61dup XP_005248576.2:n.1992-61dup
XM_011543406.1:c.2115-61dup XP_011541708.1:n.2115-61dup
XM_011543407.1:c.2091-61dup XP_011541709.1:n.2091-61dup
XM_011543408.1:c.2370-61dup XP_011541710.1:n.2370-61dup
XM_017009484.1:c.1959-61dup XP_016864973.1:n.1959-61dup
XM_017009485.1:c.1881-61dup XP_016864974.1:n.1881-61dup
XR_001742068.2:n.2401-61dup
NM_005921.2:c.2370-61dup MANE Select NP_005912.1:n.2370-61dup