Canonical Allele Identifier: CA400572507

Gene: MAP3K3 STRADA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63691212C>G , CM000679.2:g.63691212C>G	GRCh38
NC_000017.10:g.61768572C>G , CM000679.1:g.61768572C>G	GRCh37
NC_000017.9:g.59122304C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002401.5:c.1323C>G (MAP3K3) MANE Select	NP_002392.2:p.Ile441Met
ENST00000361733.8:c.1323C>G (MAP3K3) MANE Select	ENSP00000354485.4:p.Ile441Met
NM_001330431.1:c.1311C>G (MAP3K3)	NP_001317360.1:p.Ile437Met
NM_001330431.2:c.1311C>G (MAP3K3)	NP_001317360.1:p.Ile437Met
NM_001363768.1:c.1404C>G (MAP3K3)	NP_001350697.1:p.Ile468Met
NM_001363768.2:c.1404C>G (MAP3K3)	NP_001350697.1:p.Ile468Met
NM_002401.3:c.1323C>G (MAP3K3)	NP_002392.2:p.Ile441Met
NM_002401.4:c.1323C>G (MAP3K3)	NP_002392.2:p.Ile441Met
NM_203351.1:c.1416C>G (MAP3K3)	NP_976226.1:p.Ile472Met
NM_203351.2:c.1416C>G (MAP3K3)	NP_976226.1:p.Ile472Met
NM_203351.3:c.1416C>G (MAP3K3)	NP_976226.1:p.Ile472Met
ENST00000361357.7:c.1416C>G (MAP3K3)	ENSP00000354927.3:p.Ile472Met
ENST00000361733.7:c.1323C>G (MAP3K3)	ENSP00000354485.3:p.Ile441Met
ENST00000577395.5:c.1311C>G (MAP3K3)	ENSP00000462086.1:p.Ile437Met
ENST00000577597.5:c.*1148C>G (MAP3K3)	ENSP00000462917.1:n.*1148C>G
ENST00000579585.5:c.1416C>G (MAP3K3)	ENSP00000461988.1:p.Ile472Met
ENST00000581732.1:c.303C>G (MAP3K3)
ENST00000584573.5:c.1404C>G (MAP3K3)	ENSP00000464130.1:p.Ile468Met
ENST00000640870.1:c.*185-615G>C (STRADA)	ENSP00000492479.1:n.*185-615G>C
XM_005257376.2:c.1404C>G (MAP3K3)	XP_005257433.1:p.Ile468Met
XM_005257377.2:c.1311C>G (MAP3K3)	XP_005257434.1:p.Ile437Met
XM_005257378.2:c.1416C>G (MAP3K3)	XP_005257435.1:p.Ile472Met
XR_934463.1:n.2076C>G (MAP3K3)