Canonical Allele Identifier: CA2559255270
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881870_56881871insCT , CM000667.2:g.56881870_56881871insCT GRCh38
NC_000005.9:g.56177697_56177698insCT , CM000667.1:g.56177697_56177698insCT GRCh37
NC_000005.8:g.56213454_56213455insCT NCBI36
NG_031884.1:g.71798_71799insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2670_2671insCT MANE Select ENSP00000382423.3:p.Asn891LeufsTer19
ENST00000399503.3:c.2670_2671insCT ENSP00000382423.3:p.Asn891LeufsTer19
NM_005921.1:c.2670_2671insCT NP_005912.1:p.Asn891LeufsTer19
XM_005248519.3:c.2292_2293insCT XP_005248576.2:p.Asn765LeufsTer19
XM_011543406.1:c.2415_2416insCT XP_011541708.1:p.Asn806LeufsTer19
XM_011543407.1:c.2391_2392insCT XP_011541709.1:p.Asn798LeufsTer19
XM_011543408.1:c.2670_2671insCT XP_011541710.1:p.Asn891LeufsTer19
XM_017009484.1:c.2259_2260insCT XP_016864973.1:p.Asn754LeufsTer19
XM_017009485.1:c.2181_2182insCT XP_016864974.1:p.Asn728LeufsTer19
XR_001742068.2:n.2701_2702insCT
NM_005921.2:c.2670_2671insCT MANE Select NP_005912.1:p.Asn891LeufsTer19