Canonical Allele Identifier: CA2560771928

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882365_56882366insTTTTT , CM000667.2:g.56882365_56882366insTTTTT	GRCh38
NC_000005.9:g.56178192_56178193insTTTTT , CM000667.1:g.56178192_56178193insTTTTT	GRCh37
NC_000005.8:g.56213949_56213950insTTTTT	NCBI36
NG_031884.1:g.72293_72294insTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3165_3166insTTTTT MANE Select	ENSP00000382423.3:p.Asn1056PhefsTer28
ENST00000399503.3:c.3165_3166insTTTTT	ENSP00000382423.3:p.Asn1056PhefsTer28
NM_005921.1:c.3165_3166insTTTTT	NP_005912.1:p.Asn1056PhefsTer28
XM_005248519.3:c.2787_2788insTTTTT	XP_005248576.2:p.Asn930PhefsTer28
XM_011543406.1:c.2910_2911insTTTTT	XP_011541708.1:p.Asn971PhefsTer28
XM_011543407.1:c.2886_2887insTTTTT	XP_011541709.1:p.Asn963PhefsTer28
XM_011543408.1:c.3165_3166insTTTTT	XP_011541710.1:p.Asn1056PhefsTer28
XM_017009484.1:c.2754_2755insTTTTT	XP_016864973.1:p.Asn919PhefsTer28
XM_017009485.1:c.2676_2677insTTTTT	XP_016864974.1:p.Asn893PhefsTer28
XR_001742068.2:n.3196_3197insTTTTT
NM_005921.2:c.3165_3166insTTTTT MANE Select	NP_005912.1:p.Asn1056PhefsTer28