Canonical Allele Identifier: CA1548139359

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881914C= , CM000667.2:g.56881914C=	GRCh38
NC_000005.9:g.56177741C= , CM000667.1:g.56177741C=	GRCh37
NC_000005.8:g.56213498C=	NCBI36
NG_031884.1:g.71842C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2714C= MANE Select	ENSP00000382423.3:p.Thr905=
ENST00000399503.3:c.2714C=	ENSP00000382423.3:p.Thr905=
NM_005921.1:c.2714C=	NP_005912.1:p.Thr905=
XM_005248519.3:c.2336C=	XP_005248576.2:p.Thr779=
XM_011543406.1:c.2459C=	XP_011541708.1:p.Thr820=
XM_011543407.1:c.2435C=	XP_011541709.1:p.Thr812=
XM_011543408.1:c.2714C=	XP_011541710.1:p.Thr905=
XM_017009484.1:c.2303C=	XP_016864973.1:p.Thr768=
XM_017009485.1:c.2225C=	XP_016864974.1:p.Thr742=
XR_001742068.2:n.2745C=
NM_005921.2:c.2714C= MANE Select	NP_005912.1:p.Thr905=