Canonical Allele Identifier: CA365012166

Gene: MAP3K7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.90553473A>G , CM000668.2:g.90553473A>G	GRCh38
NC_000006.11:g.91263192A>G , CM000668.1:g.91263192A>G	GRCh37
NC_000006.10:g.91319913A>G	NCBI36
NG_011966.2:g.38716T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_145331.3:c.721T>C MANE Select	NP_663304.1:p.Trp241Arg
ENST00000369329.8:c.721T>C MANE Select	ENSP00000358335.3:p.Trp241Arg
NM_003188.3:c.721T>C	NP_003179.1:p.Trp241Arg
NM_003188.4:c.721T>C	NP_003179.1:p.Trp241Arg
NM_145331.2:c.721T>C	NP_663304.1:p.Trp241Arg
NM_145332.2:c.721T>C	NP_663305.1:p.Trp241Arg
NM_145332.3:c.721T>C	NP_663305.1:p.Trp241Arg
NM_145333.2:c.721T>C	NP_663306.1:p.Trp241Arg
NM_145333.3:c.721T>C	NP_663306.1:p.Trp241Arg
ENST00000369325.7:c.721T>C	ENSP00000358331.3:p.Trp241Arg
ENST00000369327.7:c.721T>C	ENSP00000358333.3:p.Trp241Arg
ENST00000369329.7:c.721T>C	ENSP00000358335.3:p.Trp241Arg
ENST00000369332.7:c.721T>C	ENSP00000358338.3:p.Trp241Arg
ENST00000700580.1:c.721T>C	ENSP00000515074.1:p.Trp241Arg
ENST00000700581.1:c.721T>C	ENSP00000515075.1:p.Trp241Arg
ENST00000700582.1:c.*576T>C	ENSP00000515076.1:n.*576T>C
ENST00000700583.1:c.*327T>C	ENSP00000515077.1:n.*327T>C
ENST00000700584.1:c.*682T>C	ENSP00000515078.1:n.*682T>C
ENST00000700587.1:c.*660T>C	ENSP00000515080.1:n.*660T>C
ENST00000700588.1:n.787T>C
ENST00000700589.1:c.721T>C	ENSP00000515081.1:p.Trp241Arg
ENST00000700590.1:n.910T>C
ENST00000700591.1:c.655T>C	ENSP00000515082.1:p.Trp219Arg
ENST00000700592.1:c.796T>C	ENSP00000515083.1:p.Trp266Arg
ENST00000700593.1:c.412T>C	ENSP00000515084.1:p.Trp138Arg
ENST00000700594.1:c.*475T>C	ENSP00000515085.1:n.*475T>C
ENST00000703100.1:c.*54T>C	ENSP00000515168.1:n.*54T>C
ENST00000703101.1:c.121-29690T>C	ENSP00000515169.1:n.121-29690T>C
XM_006715553.2:c.331T>C	XP_006715616.1:p.Trp111Arg
XM_006715553.3:c.331T>C	XP_006715616.1:p.Trp111Arg
XM_017011226.2:c.331T>C	XP_016866715.1:p.Trp111Arg