Canonical Allele Identifier: CA1548128173

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56857565_56857569delinsTTGTC , CM000667.2:g.56857565_56857569delinsTTGTC	GRCh38
NC_000005.9:g.56153392_56153396delinsTTGTC , CM000667.1:g.56153392_56153396delinsTTGTC	GRCh37
NC_000005.8:g.56189149_56189153delinsTTGTC	NCBI36
NG_031884.1:g.47493_47497delinsTTGTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.633+815_633+819delinsTTGTC MANE Select	ENSP00000382423.3:n.633+815_633+819delins...
ENST00000399503.3:c.633+815_633+819delinsTTGTC	ENSP00000382423.3:n.633+815_633+819delins...
NM_005921.1:c.633+815_633+819delinsTTGTC	NP_005912.1:n.633+815_633+819delinsTTGTC
XM_005248519.3:c.255+815_255+819delinsTTGTC	XP_005248576.2:n.255+815_255+819delinsTTG...
XM_011543406.1:c.378+815_378+819delinsTTGTC	XP_011541708.1:n.378+815_378+819delinsTTG...
XM_011543407.1:c.633+815_633+819delinsTTGTC	XP_011541709.1:n.633+815_633+819delinsTTG...
XM_011543408.1:c.633+815_633+819delinsTTGTC	XP_011541710.1:n.633+815_633+819delinsTTG...
XM_017009484.1:c.222+815_222+819delinsTTGTC	XP_016864973.1:n.222+815_222+819delinsTTG...
XM_017009485.1:c.144+815_144+819delinsTTGTC	XP_016864974.1:n.144+815_144+819delinsTTG...
XR_001742068.2:n.664+815_664+819delinsTTGTC
NM_005921.2:c.633+815_633+819delinsTTGTC MANE Select	NP_005912.1:n.633+815_633+819delinsTTGTC