Canonical Allele Identifier: CA14477069

Gene: MAP3K3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63635604T>C , CM000679.2:g.63635604T>C	GRCh38
NC_000017.10:g.61712964T>C , CM000679.1:g.61712964T>C	GRCh37
NC_000017.9:g.59066696T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002401.5:c.126+2802T>C MANE Select	NP_002392.2:n.126+2802T>C
ENST00000361733.8:c.126+2802T>C MANE Select	ENSP00000354485.4:n.126+2802T>C
NM_001330431.1:c.126+2802T>C	NP_001317360.1:n.126+2802T>C
NM_001330431.2:c.126+2802T>C	NP_001317360.1:n.126+2802T>C
NM_001363768.1:c.219+803T>C	NP_001350697.1:n.219+803T>C
NM_001363768.2:c.219+803T>C	NP_001350697.1:n.219+803T>C
NM_002401.3:c.126+2802T>C	NP_002392.2:n.126+2802T>C
NM_002401.4:c.126+2802T>C	NP_002392.2:n.126+2802T>C
NM_203351.1:c.219+803T>C	NP_976226.1:n.219+803T>C
NM_203351.2:c.219+803T>C	NP_976226.1:n.219+803T>C
NM_203351.3:c.219+803T>C	NP_976226.1:n.219+803T>C
ENST00000361357.7:c.219+803T>C	ENSP00000354927.3:n.219+803T>C
ENST00000361733.7:c.126+2802T>C	ENSP00000354485.3:n.126+2802T>C
ENST00000577395.5:c.126+2802T>C	ENSP00000462086.1:n.126+2802T>C
ENST00000577597.5:c.122+2806T>C	ENSP00000462917.1:n.122+2806T>C
ENST00000579585.5:c.219+803T>C	ENSP00000461988.1:n.219+803T>C
ENST00000584573.5:c.219+803T>C	ENSP00000464130.1:n.219+803T>C
XM_005257376.2:c.219+803T>C	XP_005257433.1:n.219+803T>C
XM_005257377.2:c.126+2802T>C	XP_005257434.1:n.126+2802T>C
XM_005257378.2:c.219+803T>C	XP_005257435.1:n.219+803T>C
XR_934463.1:n.770+803T>C