Canonical Allele Identifier: CA1548139412

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882034C= , CM000667.2:g.56882034C=	GRCh38
NC_000005.9:g.56177861C= , CM000667.1:g.56177861C=	GRCh37
NC_000005.8:g.56213618C=	NCBI36
NG_031884.1:g.71962C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2834C= MANE Select	ENSP00000382423.3:p.Thr945=
ENST00000399503.3:c.2834C=	ENSP00000382423.3:p.Thr945=
NM_005921.1:c.2834C=	NP_005912.1:p.Thr945=
XM_005248519.3:c.2456C=	XP_005248576.2:p.Thr819=
XM_011543406.1:c.2579C=	XP_011541708.1:p.Thr860=
XM_011543407.1:c.2555C=	XP_011541709.1:p.Thr852=
XM_011543408.1:c.2834C=	XP_011541710.1:p.Thr945=
XM_017009484.1:c.2423C=	XP_016864973.1:p.Thr808=
XM_017009485.1:c.2345C=	XP_016864974.1:p.Thr782=
XR_001742068.2:n.2865C=
NM_005921.2:c.2834C= MANE Select	NP_005912.1:p.Thr945=