Canonical Allele Identifier: CA1548136430

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875190T= , CM000667.2:g.56875190T=	GRCh38
NC_000005.9:g.56171017T= , CM000667.1:g.56171017T=	GRCh37
NC_000005.8:g.56206774T=	NCBI36
NG_031884.1:g.65118T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1845T= MANE Select	ENSP00000382423.3:p.Ser615=
ENST00000399503.3:c.1845T=	ENSP00000382423.3:p.Ser615=
NM_005921.1:c.1845T=	NP_005912.1:p.Ser615=
XM_005248519.3:c.1467T=	XP_005248576.2:p.Ser489=
XM_011543406.1:c.1590T=	XP_011541708.1:p.Ser530=
XM_011543407.1:c.1686+2185T=	XP_011541709.1:n.1686+2185T=
XM_011543408.1:c.1845T=	XP_011541710.1:p.Ser615=
XM_017009484.1:c.1434T=	XP_016864973.1:p.Ser478=
XM_017009485.1:c.1356T=	XP_016864974.1:p.Ser452=
XR_001742068.2:n.1876T=
NM_005921.2:c.1845T= MANE Select	NP_005912.1:p.Ser615=