Canonical Allele Identifier: CA365011779

Gene: MAP3K7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.90552101G>T , CM000668.2:g.90552101G>T	GRCh38
NC_000006.11:g.91261820G>T , CM000668.1:g.91261820G>T	GRCh37
NC_000006.10:g.91318541G>T	NCBI36
NG_011966.2:g.40088C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_145331.3:c.815C>A MANE Select	NP_663304.1:p.Ser272Tyr
ENST00000369329.8:c.815C>A MANE Select	ENSP00000358335.3:p.Ser272Tyr
NM_003188.3:c.815C>A	NP_003179.1:p.Ser272Tyr
NM_003188.4:c.815C>A	NP_003179.1:p.Ser272Tyr
NM_145331.2:c.815C>A	NP_663304.1:p.Ser272Tyr
NM_145332.2:c.815C>A	NP_663305.1:p.Ser272Tyr
NM_145332.3:c.815C>A	NP_663305.1:p.Ser272Tyr
NM_145333.2:c.815C>A	NP_663306.1:p.Ser272Tyr
NM_145333.3:c.815C>A	NP_663306.1:p.Ser272Tyr
ENST00000369320.1:c.-1642C>A	ENSP00000358326.1:n.-1642C>A
ENST00000369325.7:c.815C>A	ENSP00000358331.3:p.Ser272Tyr
ENST00000369327.7:c.815C>A	ENSP00000358333.3:p.Ser272Tyr
ENST00000369329.7:c.815C>A	ENSP00000358335.3:p.Ser272Tyr
ENST00000369332.7:c.815C>A	ENSP00000358338.3:p.Ser272Tyr
ENST00000700580.1:c.815C>A	ENSP00000515074.1:p.Ser272Tyr
ENST00000700581.1:c.815C>A	ENSP00000515075.1:p.Ser272Tyr
ENST00000700582.1:c.*670C>A	ENSP00000515076.1:n.*670C>A
ENST00000700583.1:c.*421C>A	ENSP00000515077.1:n.*421C>A
ENST00000700584.1:c.*776C>A	ENSP00000515078.1:n.*776C>A
ENST00000700587.1:c.*754C>A	ENSP00000515080.1:n.*754C>A
ENST00000700588.1:n.881C>A
ENST00000700589.1:c.*219C>A	ENSP00000515081.1:n.*219C>A
ENST00000700590.1:n.1004C>A
ENST00000700591.1:c.749C>A	ENSP00000515082.1:p.Ser250Tyr
ENST00000700592.1:c.890C>A	ENSP00000515083.1:p.Ser297Tyr
ENST00000700593.1:c.506C>A	ENSP00000515084.1:p.Ser169Tyr
ENST00000700594.1:c.*569C>A	ENSP00000515085.1:n.*569C>A
ENST00000703100.1:c.*148C>A	ENSP00000515168.1:n.*148C>A
ENST00000703101.1:c.121-28318C>A	ENSP00000515169.1:n.121-28318C>A
XM_006715553.2:c.425C>A	XP_006715616.1:p.Ser142Tyr
XM_006715553.3:c.425C>A	XP_006715616.1:p.Ser142Tyr
XM_017011226.2:c.425C>A	XP_016866715.1:p.Ser142Tyr