Canonical Allele Identifier: CA2708943398
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs2111873450

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859666dup , CM000667.2:g.56859666dup GRCh38
NC_000005.9:g.56155493dup , CM000667.1:g.56155493dup GRCh37
NC_000005.8:g.56191250dup NCBI36
NG_031884.1:g.49594dup

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.634-49dup MANE Select ENSP00000382423.3:n.634-49dup
ENST00000399503.3:c.634-49dup ENSP00000382423.3:n.634-49dup
NM_005921.1:c.634-49dup NP_005912.1:n.634-49dup
XM_005248519.3:c.256-49dup XP_005248576.2:n.256-49dup
XM_011543406.1:c.379-49dup XP_011541708.1:n.379-49dup
XM_011543407.1:c.634-49dup XP_011541709.1:n.634-49dup
XM_011543408.1:c.634-49dup XP_011541710.1:n.634-49dup
XM_017009484.1:c.223-49dup XP_016864973.1:n.223-49dup
XM_017009485.1:c.145-49dup XP_016864974.1:n.145-49dup
XR_001742068.2:n.665-49dup
NM_005921.2:c.634-49dup MANE Select NP_005912.1:n.634-49dup