Canonical Allele Identifier: CA2597564041
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs2111875054

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859977_56859980del , CM000667.2:g.56859977_56859980del GRCh38
NC_000005.9:g.56155804_56155807del , CM000667.1:g.56155804_56155807del GRCh37
NC_000005.8:g.56191561_56191564del NCBI36
NG_031884.1:g.49905_49908del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.834+62_834+65del MANE Select ENSP00000382423.3:n.834+62_834+65del
ENST00000399503.3:c.834+62_834+65del ENSP00000382423.3:n.834+62_834+65del
NM_005921.1:c.834+62_834+65del NP_005912.1:n.834+62_834+65del
XM_005248519.3:c.456+62_456+65del XP_005248576.2:n.456+62_456+65del
XM_011543406.1:c.579+62_579+65del XP_011541708.1:n.579+62_579+65del
XM_011543407.1:c.834+62_834+65del XP_011541709.1:n.834+62_834+65del
XM_011543408.1:c.834+62_834+65del XP_011541710.1:n.834+62_834+65del
XM_017009484.1:c.423+62_423+65del XP_016864973.1:n.423+62_423+65del
XM_017009485.1:c.345+62_345+65del XP_016864974.1:n.345+62_345+65del
XR_001742068.2:n.865+62_865+65del
NM_005921.2:c.834+62_834+65del MANE Select NP_005912.1:n.834+62_834+65del