Canonical Allele Identifier: CA1548136439

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875211T= , CM000667.2:g.56875211T=	GRCh38
NC_000005.9:g.56171038T= , CM000667.1:g.56171038T=	GRCh37
NC_000005.8:g.56206795T=	NCBI36
NG_031884.1:g.65139T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.1866T= MANE Select	ENSP00000382423.3:p.Ser622=
ENST00000399503.3:c.1866T=	ENSP00000382423.3:p.Ser622=
NM_005921.1:c.1866T=	NP_005912.1:p.Ser622=
XM_005248519.3:c.1488T=	XP_005248576.2:p.Ser496=
XM_011543406.1:c.1611T=	XP_011541708.1:p.Ser537=
XM_011543407.1:c.1686+2206T=	XP_011541709.1:n.1686+2206T=
XM_011543408.1:c.1866T=	XP_011541710.1:p.Ser622=
XM_017009484.1:c.1455T=	XP_016864973.1:p.Ser485=
XM_017009485.1:c.1377T=	XP_016864974.1:p.Ser459=
XR_001742068.2:n.1897T=
NM_005921.2:c.1866T= MANE Select	NP_005912.1:p.Ser622=