Canonical Allele Identifier: CA1548128142
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56857485_56857488delinsTTTG , CM000667.2:g.56857485_56857488delinsTTTG GRCh38
NC_000005.9:g.56153312_56153315delinsTTTG , CM000667.1:g.56153312_56153315delinsTTTG GRCh37
NC_000005.8:g.56189069_56189072delinsTTTG NCBI36
NG_031884.1:g.47413_47416delinsTTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.633+735_633+738delinsTTTG MANE Select ENSP00000382423.3:n.633+735_633+738delins...
ENST00000399503.3:c.633+735_633+738delinsTTTG ENSP00000382423.3:n.633+735_633+738delins...
NM_005921.1:c.633+735_633+738delinsTTTG NP_005912.1:n.633+735_633+738delinsTTTG
XM_005248519.3:c.255+735_255+738delinsTTTG XP_005248576.2:n.255+735_255+738delinsTTT...
XM_011543406.1:c.378+735_378+738delinsTTTG XP_011541708.1:n.378+735_378+738delinsTTT...
XM_011543407.1:c.633+735_633+738delinsTTTG XP_011541709.1:n.633+735_633+738delinsTTT...
XM_011543408.1:c.633+735_633+738delinsTTTG XP_011541710.1:n.633+735_633+738delinsTTT...
XM_017009484.1:c.222+735_222+738delinsTTTG XP_016864973.1:n.222+735_222+738delinsTTT...
XM_017009485.1:c.144+735_144+738delinsTTTG XP_016864974.1:n.144+735_144+738delinsTTT...
XR_001742068.2:n.664+735_664+738delinsTTTG
NM_005921.2:c.633+735_633+738delinsTTTG MANE Select NP_005912.1:n.633+735_633+738delinsTTTG