Canonical Allele Identifier: CA8702807

Gene: MAP3K3 STRADA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63692327G>A , CM000679.2:g.63692327G>A	GRCh38
NC_000017.10:g.61769687G>A , CM000679.1:g.61769687G>A	GRCh37
NC_000017.9:g.59123419G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002401.5:c.1560G>A (MAP3K3) MANE Select	NP_002392.2:p.Ser520=
ENST00000361733.8:c.1560G>A (MAP3K3) MANE Select	ENSP00000354485.4:p.Ser520=
NM_001330431.1:c.1548G>A (MAP3K3)	NP_001317360.1:p.Ser516=
NM_001330431.2:c.1548G>A (MAP3K3)	NP_001317360.1:p.Ser516=
NM_001363768.1:c.1641G>A (MAP3K3)	NP_001350697.1:p.Ser547=
NM_001363768.2:c.1641G>A (MAP3K3)	NP_001350697.1:p.Ser547=
NM_002401.3:c.1560G>A (MAP3K3)	NP_002392.2:p.Ser520=
NM_002401.4:c.1560G>A (MAP3K3)	NP_002392.2:p.Ser520=
NM_203351.1:c.1653G>A (MAP3K3)	NP_976226.1:p.Ser551=
NM_203351.2:c.1653G>A (MAP3K3)	NP_976226.1:p.Ser551=
NM_203351.3:c.1653G>A (MAP3K3)	NP_976226.1:p.Ser551=
ENST00000361357.7:c.1653G>A (MAP3K3)	ENSP00000354927.3:p.Ser551=
ENST00000361733.7:c.1560G>A (MAP3K3)	ENSP00000354485.3:p.Ser520=
ENST00000577395.5:c.1548G>A (MAP3K3)	ENSP00000462086.1:p.Ser516=
ENST00000577597.5:c.*1385G>A (MAP3K3)	ENSP00000462917.1:n.*1385G>A
ENST00000579585.5:c.1653G>A (MAP3K3)	ENSP00000461988.1:p.Ser551=
ENST00000581732.1:c.540G>A (MAP3K3)
ENST00000584573.5:c.1641G>A (MAP3K3)	ENSP00000464130.1:p.Ser547=
ENST00000640870.1:c.*185-1730C>T (STRADA)	ENSP00000492479.1:n.*185-1730C>T
XM_005257376.2:c.1641G>A (MAP3K3)	XP_005257433.1:p.Ser547=
XM_005257377.2:c.1548G>A (MAP3K3)	XP_005257434.1:p.Ser516=
XM_005257378.2:c.1567+465G>A (MAP3K3)	XP_005257435.1:n.1567+465G>A
XR_934463.1:n.2313G>A (MAP3K3)