Canonical Allele Identifier: CA400566142

Gene: MAP3K3 STRADA

Linked Data

• MyVariant Identifiers: chr17:g.61762938G>T (hg19) ; chr17:g.63685578G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63685578G>T , CM000679.2:g.63685578G>T	GRCh38
NC_000017.10:g.61762938G>T , CM000679.1:g.61762938G>T	GRCh37
NC_000017.9:g.59116670G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361733.8:c.698G>T (MAP3K3) MANE Select	ENSP00000354485.4:p.Arg233Met
ENST00000640870.1:c.*393-2820C>A (STRADA)	ENSP00000492479.1:n.*393-2820C>A
ENST00000361357.7:c.791G>T (MAP3K3)	ENSP00000354927.3:p.Arg264Met
ENST00000361733.7:c.698G>T (MAP3K3)	ENSP00000354485.3:p.Arg233Met
ENST00000577395.5:c.698G>T (MAP3K3)	ENSP00000462086.1:p.Ser233Ile
ENST00000577597.5:c.*523G>T (MAP3K3)	ENSP00000462917.1:n.*523G>T
ENST00000579585.5:c.791G>T (MAP3K3)	ENSP00000461988.1:p.Arg264Met
ENST00000584573.5:c.791G>T (MAP3K3)	ENSP00000464130.1:p.Ser264Ile
ENST00000585302.1:c.530G>T (MAP3K3)
NM_002401.3:c.698G>T (MAP3K3)	NP_002392.2:p.Arg233Met
NM_203351.1:c.791G>T (MAP3K3)	NP_976226.1:p.Arg264Met
XM_005257376.2:c.791G>T (MAP3K3)	XP_005257433.1:p.Ser264Ile
XM_005257377.2:c.698G>T (MAP3K3)	XP_005257434.1:p.Ser233Ile
XM_005257378.2:c.791G>T (MAP3K3)	XP_005257435.1:p.Arg264Met
XR_243740.2:n.594-2820C>A
XR_934463.1:n.1342G>T (MAP3K3)
NM_001330431.1:c.698G>T (MAP3K3)	NP_001317360.1:p.Ser233Ile
NM_001363768.1:c.791G>T (MAP3K3)	NP_001350697.1:p.Ser264Ile
NM_002401.4:c.698G>T (MAP3K3)	NP_002392.2:p.Arg233Met
NM_203351.2:c.791G>T (MAP3K3)	NP_976226.1:p.Arg264Met
XR_243740.3:n.613-2820C>A
NM_001330431.2:c.698G>T (MAP3K3)	NP_001317360.1:p.Ser233Ile
NM_001363768.2:c.791G>T (MAP3K3)	NP_001350697.1:p.Ser264Ile
NM_002401.5:c.698G>T (MAP3K3) MANE Select	NP_002392.2:p.Arg233Met
NM_203351.3:c.791G>T (MAP3K3)	NP_976226.1:p.Arg264Met