Canonical Allele Identifier: CA143017447

Gene: MAP3K7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.90568607C>T , CM000668.2:g.90568607C>T	GRCh38
NC_000006.11:g.91278326C>T , CM000668.1:g.91278326C>T	GRCh37
NC_000006.10:g.91335047C>T	NCBI36
NG_011966.2:g.23582G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_145331.3:c.248G>A MANE Select	NP_663304.1:p.Arg83His
ENST00000369329.8:c.248G>A MANE Select	ENSP00000358335.3:p.Arg83His
NM_003188.3:c.248G>A	NP_003179.1:p.Arg83His
NM_003188.4:c.248G>A	NP_003179.1:p.Arg83His
NM_145331.2:c.248G>A	NP_663304.1:p.Arg83His
NM_145332.2:c.248G>A	NP_663305.1:p.Arg83His
NM_145332.3:c.248G>A	NP_663305.1:p.Arg83His
NM_145333.2:c.248G>A	NP_663306.1:p.Arg83His
NM_145333.3:c.248G>A	NP_663306.1:p.Arg83His
ENST00000369325.7:c.248G>A	ENSP00000358331.3:p.Arg83His
ENST00000369327.7:c.248G>A	ENSP00000358333.3:p.Arg83His
ENST00000369329.7:c.248G>A	ENSP00000358335.3:p.Arg83His
ENST00000369332.7:c.248G>A	ENSP00000358338.3:p.Arg83His
ENST00000700580.1:c.248G>A	ENSP00000515074.1:p.Arg83His
ENST00000700581.1:c.248G>A	ENSP00000515075.1:p.Arg83His
ENST00000700582.1:c.248G>A	ENSP00000515076.1:p.Arg83His
ENST00000700583.1:c.248G>A	ENSP00000515077.1:p.Arg83His
ENST00000700584.1:c.*209G>A	ENSP00000515078.1:n.*209G>A
ENST00000700587.1:c.*187G>A	ENSP00000515080.1:n.*187G>A
ENST00000700588.1:n.314G>A
ENST00000700589.1:c.248G>A	ENSP00000515081.1:p.Arg83His
ENST00000700590.1:n.437G>A
ENST00000700591.1:c.231+3090G>A	ENSP00000515082.1:n.231+3090G>A
ENST00000700592.1:c.323G>A	ENSP00000515083.1:p.Arg108His
ENST00000700593.1:c.-62G>A	ENSP00000515084.1:n.-62G>A
ENST00000700594.1:c.248G>A	ENSP00000515085.1:p.Arg83His
ENST00000703100.1:c.248G>A	ENSP00000515168.1:p.Arg83His
ENST00000703101.1:c.120+18157G>A	ENSP00000515169.1:n.120+18157G>A
XM_006715553.2:c.-163G>A	XP_006715616.1:n.-163G>A
XM_006715553.3:c.-163G>A	XP_006715616.1:n.-163G>A
XM_017011226.2:c.-163G>A	XP_016866715.1:n.-163G>A