Canonical Allele Identifier: CA400566146

Gene: MAP3K3 STRADA

Linked Data

• gnomAD v4: 17-63685579-G-A
• MyVariant Identifiers: chr17:g.61762939G>A (hg19) ; chr17:g.63685579G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63685579G>A , CM000679.2:g.63685579G>A	GRCh38
NC_000017.10:g.61762939G>A , CM000679.1:g.61762939G>A	GRCh37
NC_000017.9:g.59116671G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361733.8:c.699G>A (MAP3K3) MANE Select	ENSP00000354485.4:p.Arg233=
ENST00000640870.1:c.*393-2821C>T (STRADA)	ENSP00000492479.1:n.*393-2821C>T
ENST00000361357.7:c.792G>A (MAP3K3)	ENSP00000354927.3:p.Arg264=
ENST00000361733.7:c.699G>A (MAP3K3)	ENSP00000354485.3:p.Arg233=
ENST00000577395.5:c.698+1G>A (MAP3K3)	ENSP00000462086.1:n.698+1G>A
ENST00000577597.5:c.*524G>A (MAP3K3)	ENSP00000462917.1:n.*524G>A
ENST00000579585.5:c.792G>A (MAP3K3)	ENSP00000461988.1:p.Arg264=
ENST00000584573.5:c.791+1G>A (MAP3K3)	ENSP00000464130.1:n.791+1G>A
ENST00000585302.1:c.530+1G>A (MAP3K3)
NM_002401.3:c.699G>A (MAP3K3)	NP_002392.2:p.Arg233=
NM_203351.1:c.792G>A (MAP3K3)	NP_976226.1:p.Arg264=
XM_005257376.2:c.791+1G>A (MAP3K3)	XP_005257433.1:n.791+1G>A
XM_005257377.2:c.698+1G>A (MAP3K3)	XP_005257434.1:n.698+1G>A
XM_005257378.2:c.792G>A (MAP3K3)	XP_005257435.1:p.Arg264=
XR_243740.2:n.594-2821C>T
XR_934463.1:n.1343G>A (MAP3K3)
NM_001330431.1:c.698+1G>A (MAP3K3)	NP_001317360.1:n.698+1G>A
NM_001363768.1:c.791+1G>A (MAP3K3)	NP_001350697.1:n.791+1G>A
NM_002401.4:c.699G>A (MAP3K3)	NP_002392.2:p.Arg233=
NM_203351.2:c.792G>A (MAP3K3)	NP_976226.1:p.Arg264=
XR_243740.3:n.613-2821C>T
NM_001330431.2:c.698+1G>A (MAP3K3)	NP_001317360.1:n.698+1G>A
NM_001363768.2:c.791+1G>A (MAP3K3)	NP_001350697.1:n.791+1G>A
NM_002401.5:c.699G>A (MAP3K3) MANE Select	NP_002392.2:p.Arg233=
NM_203351.3:c.792G>A (MAP3K3)	NP_976226.1:p.Arg264=