Canonical Allele Identifier: CA365015152

Gene: MAP3K7

Linked Data

• MyVariant Identifiers: chr6:g.91228277A>T (hg19) ; chr6:g.90518558A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.90518558A>T , CM000668.2:g.90518558A>T	GRCh38
NC_000006.11:g.91228277A>T , CM000668.1:g.91228277A>T	GRCh37
NC_000006.10:g.91284998A>T	NCBI36
NG_011966.2:g.73631T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700580.1:c.1448T>A	ENSP00000515074.1:p.Leu483Gln
ENST00000700581.1:c.*670T>A	ENSP00000515075.1:n.*670T>A
ENST00000700582.1:c.*1384T>A	ENSP00000515076.1:n.*1384T>A
ENST00000700583.1:c.*1054T>A	ENSP00000515077.1:n.*1054T>A
ENST00000700584.1:c.*1409T>A	ENSP00000515078.1:n.*1409T>A
ENST00000700585.1:c.489T>A	ENSP00000515079.1:n.489T>A
ENST00000700586.1:n.1199T>A
ENST00000700587.1:c.*1468T>A	ENSP00000515080.1:n.*1468T>A
ENST00000700588.1:n.1514T>A
ENST00000700589.1:c.*852T>A	ENSP00000515081.1:n.*852T>A
ENST00000700591.1:c.1382T>A	ENSP00000515082.1:p.Leu461Gln
ENST00000700592.1:c.1523T>A	ENSP00000515083.1:p.Leu508Gln
ENST00000700593.1:c.1139T>A	ENSP00000515084.1:p.Leu380Gln
ENST00000700594.1:c.*1283T>A	ENSP00000515085.1:n.*1283T>A
ENST00000703099.1:n.995T>A
ENST00000703100.1:c.*862T>A	ENSP00000515168.1:n.*862T>A
ENST00000703101.1:c.293T>A	ENSP00000515169.1:p.Leu98Gln
ENST00000369329.8:c.1529T>A MANE Select	ENSP00000358335.3:p.Leu510Gln
ENST00000369320.1:c.491T>A	ENSP00000358326.1:p.Leu164Gln
ENST00000369325.7:c.1524+700T>A	ENSP00000358331.3:n.1524+700T>A
ENST00000369327.7:c.1443+700T>A	ENSP00000358333.3:n.1443+700T>A
ENST00000369329.7:c.1529T>A	ENSP00000358335.3:p.Leu510Gln
ENST00000369332.7:c.1448T>A	ENSP00000358338.3:p.Leu483Gln
ENST00000479630.1:n.1055T>A
NM_003188.3:c.1448T>A	NP_003179.1:p.Leu483Gln
NM_145331.2:c.1529T>A	NP_663304.1:p.Leu510Gln
NM_145332.2:c.1524+700T>A	NP_663305.1:n.1524+700T>A
NM_145333.2:c.1443+700T>A	NP_663306.1:n.1443+700T>A
XM_006715553.2:c.1139T>A	XP_006715616.1:p.Leu380Gln
XM_006715553.3:c.1139T>A	XP_006715616.1:p.Leu380Gln
XM_017011226.2:c.1058T>A	XP_016866715.1:p.Leu353Gln
NM_145331.3:c.1529T>A MANE Select	NP_663304.1:p.Leu510Gln
NM_003188.4:c.1448T>A	NP_003179.1:p.Leu483Gln
NM_145332.3:c.1524+700T>A	NP_663305.1:n.1524+700T>A
NM_145333.3:c.1443+700T>A	NP_663306.1:n.1443+700T>A