Canonical Allele Identifier: CA451202033

Gene: MAP3K7

Linked Data

• MyVariant Identifiers: chr6:g.91228279A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.90518560A>G , CM000668.2:g.90518560A>G	GRCh38
NC_000006.11:g.91228279A>G , CM000668.1:g.91228279A>G	GRCh37
NC_000006.10:g.91285000A>G	NCBI36
NG_011966.2:g.73629T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700580.1:c.1446T>C	ENSP00000515074.1:p.Pro482=
ENST00000700581.1:c.*668T>C	ENSP00000515075.1:n.*668T>C
ENST00000700582.1:c.*1382T>C	ENSP00000515076.1:n.*1382T>C
ENST00000700583.1:c.*1052T>C	ENSP00000515077.1:n.*1052T>C
ENST00000700584.1:c.*1407T>C	ENSP00000515078.1:n.*1407T>C
ENST00000700585.1:c.487T>C	ENSP00000515079.1:n.487T>C
ENST00000700586.1:n.1197T>C
ENST00000700587.1:c.*1466T>C	ENSP00000515080.1:n.*1466T>C
ENST00000700588.1:n.1512T>C
ENST00000700589.1:c.*850T>C	ENSP00000515081.1:n.*850T>C
ENST00000700591.1:c.1380T>C	ENSP00000515082.1:p.Pro460=
ENST00000700592.1:c.1521T>C	ENSP00000515083.1:p.Pro507=
ENST00000700593.1:c.1137T>C	ENSP00000515084.1:p.Pro379=
ENST00000700594.1:c.*1281T>C	ENSP00000515085.1:n.*1281T>C
ENST00000703099.1:n.993T>C
ENST00000703100.1:c.*860T>C	ENSP00000515168.1:n.*860T>C
ENST00000703101.1:c.291T>C	ENSP00000515169.1:p.Pro97=
ENST00000369329.8:c.1527T>C MANE Select	ENSP00000358335.3:p.Pro509=
ENST00000369320.1:c.489T>C	ENSP00000358326.1:p.Pro163=
ENST00000369325.7:c.1524+698T>C	ENSP00000358331.3:n.1524+698T>C
ENST00000369327.7:c.1443+698T>C	ENSP00000358333.3:n.1443+698T>C
ENST00000369329.7:c.1527T>C	ENSP00000358335.3:p.Pro509=
ENST00000369332.7:c.1446T>C	ENSP00000358338.3:p.Pro482=
ENST00000479630.1:n.1053T>C
NM_003188.3:c.1446T>C	NP_003179.1:p.Pro482=
NM_145331.2:c.1527T>C	NP_663304.1:p.Pro509=
NM_145332.2:c.1524+698T>C	NP_663305.1:n.1524+698T>C
NM_145333.2:c.1443+698T>C	NP_663306.1:n.1443+698T>C
XM_006715553.2:c.1137T>C	XP_006715616.1:p.Pro379=
XM_006715553.3:c.1137T>C	XP_006715616.1:p.Pro379=
XM_017011226.2:c.1056T>C	XP_016866715.1:p.Pro352=
NM_145331.3:c.1527T>C MANE Select	NP_663304.1:p.Pro509=
NM_003188.4:c.1446T>C	NP_003179.1:p.Pro482=
NM_145332.3:c.1524+698T>C	NP_663305.1:n.1524+698T>C
NM_145333.3:c.1443+698T>C	NP_663306.1:n.1443+698T>C