Canonical Allele Identifier: CA400566102

Gene: MAP3K3 STRADA

Linked Data

• MyVariant Identifiers: chr17:g.61762931T>A (hg19) ; chr17:g.63685571T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63685571T>A , CM000679.2:g.63685571T>A	GRCh38
NC_000017.10:g.61762931T>A , CM000679.1:g.61762931T>A	GRCh37
NC_000017.9:g.59116663T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361733.8:c.691T>A (MAP3K3) MANE Select	ENSP00000354485.4:p.Leu231Met
ENST00000640870.1:c.*393-2813A>T (STRADA)	ENSP00000492479.1:n.*393-2813A>T
ENST00000361357.7:c.784T>A (MAP3K3)	ENSP00000354927.3:p.Leu262Met
ENST00000361733.7:c.691T>A (MAP3K3)	ENSP00000354485.3:p.Leu231Met
ENST00000577395.5:c.691T>A (MAP3K3)	ENSP00000462086.1:p.Leu231Met
ENST00000577597.5:c.*516T>A (MAP3K3)	ENSP00000462917.1:n.*516T>A
ENST00000579585.5:c.784T>A (MAP3K3)	ENSP00000461988.1:p.Leu262Met
ENST00000584573.5:c.784T>A (MAP3K3)	ENSP00000464130.1:p.Leu262Met
ENST00000585302.1:c.523T>A (MAP3K3)
NM_002401.3:c.691T>A (MAP3K3)	NP_002392.2:p.Leu231Met
NM_203351.1:c.784T>A (MAP3K3)	NP_976226.1:p.Leu262Met
XM_005257376.2:c.784T>A (MAP3K3)	XP_005257433.1:p.Leu262Met
XM_005257377.2:c.691T>A (MAP3K3)	XP_005257434.1:p.Leu231Met
XM_005257378.2:c.784T>A (MAP3K3)	XP_005257435.1:p.Leu262Met
XR_243740.2:n.594-2813A>T
XR_934463.1:n.1335T>A (MAP3K3)
NM_001330431.1:c.691T>A (MAP3K3)	NP_001317360.1:p.Leu231Met
NM_001363768.1:c.784T>A (MAP3K3)	NP_001350697.1:p.Leu262Met
NM_002401.4:c.691T>A (MAP3K3)	NP_002392.2:p.Leu231Met
NM_203351.2:c.784T>A (MAP3K3)	NP_976226.1:p.Leu262Met
XR_243740.3:n.613-2813A>T
NM_001330431.2:c.691T>A (MAP3K3)	NP_001317360.1:p.Leu231Met
NM_001363768.2:c.784T>A (MAP3K3)	NP_001350697.1:p.Leu262Met
NM_002401.5:c.691T>A (MAP3K3) MANE Select	NP_002392.2:p.Leu231Met
NM_203351.3:c.784T>A (MAP3K3)	NP_976226.1:p.Leu262Met