Canonical Allele Identifier: CA812365424
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs1227183772

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859976del , CM000667.2:g.56859976del GRCh38
NC_000005.9:g.56155803del , CM000667.1:g.56155803del GRCh37
NC_000005.8:g.56191560del NCBI36
NG_031884.1:g.49904del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.834+61del MANE Select ENSP00000382423.3:n.834+61del
ENST00000399503.3:c.834+61del ENSP00000382423.3:n.834+61del
NM_005921.1:c.834+61del NP_005912.1:n.834+61del
XM_005248519.3:c.456+61del XP_005248576.2:n.456+61del
XM_011543406.1:c.579+61del XP_011541708.1:n.579+61del
XM_011543407.1:c.834+61del XP_011541709.1:n.834+61del
XM_011543408.1:c.834+61del XP_011541710.1:n.834+61del
XM_017009484.1:c.423+61del XP_016864973.1:n.423+61del
XM_017009485.1:c.345+61del XP_016864974.1:n.345+61del
XR_001742068.2:n.865+61del
NM_005921.2:c.834+61del MANE Select NP_005912.1:n.834+61del