Canonical Allele Identifier: CA1548129240

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859853_56859862delinsTCAGGTCGCA , CM000667.2:g.56859853_56859862delinsTCAGGTCGCA	GRCh38
NC_000005.9:g.56155680_56155689delinsTCAGGTCGCA , CM000667.1:g.56155680_56155689delinsTCAGGTCGCA	GRCh37
NC_000005.8:g.56191437_56191446delinsTCAGGTCGCA	NCBI36
NG_031884.1:g.49781_49790delinsTCAGGTCGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.772_781delinsTCAGGTCGCA MANE Select	ENSP00000382423.3:p.Ser258=
ENST00000399503.3:c.772_781delinsTCAGGTCGCA	ENSP00000382423.3:p.Ser258=
NM_005921.1:c.772_781delinsTCAGGTCGCA	NP_005912.1:p.Ser258=
XM_005248519.3:c.394_403delinsTCAGGTCGCA	XP_005248576.2:p.Ser132=
XM_011543406.1:c.517_526delinsTCAGGTCGCA	XP_011541708.1:p.Ser173=
XM_011543407.1:c.772_781delinsTCAGGTCGCA	XP_011541709.1:p.Ser258=
XM_011543408.1:c.772_781delinsTCAGGTCGCA	XP_011541710.1:p.Ser258=
XM_017009484.1:c.361_370delinsTCAGGTCGCA	XP_016864973.1:p.Ser121=
XM_017009485.1:c.283_292delinsTCAGGTCGCA	XP_016864974.1:p.Ser95=
XR_001742068.2:n.803_812delinsTCAGGTCGCA
NM_005921.2:c.772_781delinsTCAGGTCGCA MANE Select	NP_005912.1:p.Ser258=