Canonical Allele Identifier: CA645557018
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882094_56882097dup , CM000667.2:g.56882094_56882097dup GRCh38
NC_000005.9:g.56177921_56177924dup , CM000667.1:g.56177921_56177924dup GRCh37
NC_000005.8:g.56213678_56213681dup NCBI36
NG_031884.1:g.72022_72025dup

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.2894_2897dup MANE Select ENSP00000382423.3:p.Cys966Ter
ENST00000399503.3:c.2894_2897dup ENSP00000382423.3:p.Cys966Ter
NM_005921.1:c.2894_2897dup NP_005912.1:p.Cys966Ter
XM_005248519.3:c.2516_2519dup XP_005248576.2:p.Cys840Ter
XM_011543406.1:c.2639_2642dup XP_011541708.1:p.Cys881Ter
XM_011543407.1:c.2615_2618dup XP_011541709.1:p.Cys873Ter
XM_011543408.1:c.2894_2897dup XP_011541710.1:p.Cys966Ter
XM_017009484.1:c.2483_2486dup XP_016864973.1:p.Cys829Ter
XM_017009485.1:c.2405_2408dup XP_016864974.1:p.Cys803Ter
XR_001742068.2:n.2925_2928dup
NM_005921.2:c.2894_2897dup MANE Select NP_005912.1:p.Cys966Ter