Canonical Allele Identifier: CA365012676

Gene: MAP3K7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.90553578A>C , CM000668.2:g.90553578A>C	GRCh38
NC_000006.11:g.91263297A>C , CM000668.1:g.91263297A>C	GRCh37
NC_000006.10:g.91320018A>C	NCBI36
NG_011966.2:g.38611T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_145331.3:c.616T>G MANE Select	NP_663304.1:p.Tyr206Asp
ENST00000369329.8:c.616T>G MANE Select	ENSP00000358335.3:p.Tyr206Asp
NM_003188.3:c.616T>G	NP_003179.1:p.Tyr206Asp
NM_003188.4:c.616T>G	NP_003179.1:p.Tyr206Asp
NM_145331.2:c.616T>G	NP_663304.1:p.Tyr206Asp
NM_145332.2:c.616T>G	NP_663305.1:p.Tyr206Asp
NM_145332.3:c.616T>G	NP_663305.1:p.Tyr206Asp
NM_145333.2:c.616T>G	NP_663306.1:p.Tyr206Asp
NM_145333.3:c.616T>G	NP_663306.1:p.Tyr206Asp
ENST00000369325.7:c.616T>G	ENSP00000358331.3:p.Tyr206Asp
ENST00000369327.7:c.616T>G	ENSP00000358333.3:p.Tyr206Asp
ENST00000369329.7:c.616T>G	ENSP00000358335.3:p.Tyr206Asp
ENST00000369332.7:c.616T>G	ENSP00000358338.3:p.Tyr206Asp
ENST00000700580.1:c.616T>G	ENSP00000515074.1:p.Tyr206Asp
ENST00000700581.1:c.616T>G	ENSP00000515075.1:p.Tyr206Asp
ENST00000700582.1:c.*471T>G	ENSP00000515076.1:n.*471T>G
ENST00000700583.1:c.*222T>G	ENSP00000515077.1:n.*222T>G
ENST00000700584.1:c.*577T>G	ENSP00000515078.1:n.*577T>G
ENST00000700587.1:c.*555T>G	ENSP00000515080.1:n.*555T>G
ENST00000700588.1:n.682T>G
ENST00000700589.1:c.616T>G	ENSP00000515081.1:p.Tyr206Asp
ENST00000700590.1:n.805T>G
ENST00000700591.1:c.550T>G	ENSP00000515082.1:p.Tyr184Asp
ENST00000700592.1:c.691T>G	ENSP00000515083.1:p.Tyr231Asp
ENST00000700593.1:c.307T>G	ENSP00000515084.1:p.Tyr103Asp
ENST00000700594.1:c.*370T>G	ENSP00000515085.1:n.*370T>G
ENST00000703100.1:c.612T>G	ENSP00000515168.1:p.Ile204Met
ENST00000703101.1:c.121-29795T>G	ENSP00000515169.1:n.121-29795T>G
XM_006715553.2:c.226T>G	XP_006715616.1:p.Tyr76Asp
XM_006715553.3:c.226T>G	XP_006715616.1:p.Tyr76Asp
XM_017011226.2:c.226T>G	XP_016866715.1:p.Tyr76Asp