Canonical Allele Identifier: CA2673908381
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859979_56859983del , CM000667.2:g.56859979_56859983del GRCh38
NC_000005.9:g.56155806_56155810del , CM000667.1:g.56155806_56155810del GRCh37
NC_000005.8:g.56191563_56191567del NCBI36
NG_031884.1:g.49907_49911del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.834+64_834+68del MANE Select ENSP00000382423.3:n.834+64_834+68del
ENST00000399503.3:c.834+64_834+68del ENSP00000382423.3:n.834+64_834+68del
NM_005921.1:c.834+64_834+68del NP_005912.1:n.834+64_834+68del
XM_005248519.3:c.456+64_456+68del XP_005248576.2:n.456+64_456+68del
XM_011543406.1:c.579+64_579+68del XP_011541708.1:n.579+64_579+68del
XM_011543407.1:c.834+64_834+68del XP_011541709.1:n.834+64_834+68del
XM_011543408.1:c.834+64_834+68del XP_011541710.1:n.834+64_834+68del
XM_017009484.1:c.423+64_423+68del XP_016864973.1:n.423+64_423+68del
XM_017009485.1:c.345+64_345+68del XP_016864974.1:n.345+64_345+68del
XR_001742068.2:n.865+64_865+68del
NM_005921.2:c.834+64_834+68del MANE Select NP_005912.1:n.834+64_834+68del