Canonical Allele Identifier: CA365015142

Gene: MAP3K7

Linked Data

• MyVariant Identifiers: chr6:g.91228275C>A (hg19) ; chr6:g.90518556C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.90518556C>A , CM000668.2:g.90518556C>A	GRCh38
NC_000006.11:g.91228275C>A , CM000668.1:g.91228275C>A	GRCh37
NC_000006.10:g.91284996C>A	NCBI36
NG_011966.2:g.73633G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700580.1:c.1450G>T	ENSP00000515074.1:p.Ala484Ser
ENST00000700581.1:c.*672G>T	ENSP00000515075.1:n.*672G>T
ENST00000700582.1:c.*1386G>T	ENSP00000515076.1:n.*1386G>T
ENST00000700583.1:c.*1056G>T	ENSP00000515077.1:n.*1056G>T
ENST00000700584.1:c.*1411G>T	ENSP00000515078.1:n.*1411G>T
ENST00000700585.1:c.491G>T	ENSP00000515079.1:n.491G>T
ENST00000700586.1:n.1201G>T
ENST00000700587.1:c.*1470G>T	ENSP00000515080.1:n.*1470G>T
ENST00000700588.1:n.1516G>T
ENST00000700589.1:c.*854G>T	ENSP00000515081.1:n.*854G>T
ENST00000700591.1:c.1384G>T	ENSP00000515082.1:p.Ala462Ser
ENST00000700592.1:c.1525G>T	ENSP00000515083.1:p.Ala509Ser
ENST00000700593.1:c.1141G>T	ENSP00000515084.1:p.Ala381Ser
ENST00000700594.1:c.*1285G>T	ENSP00000515085.1:n.*1285G>T
ENST00000703099.1:n.997G>T
ENST00000703100.1:c.*864G>T	ENSP00000515168.1:n.*864G>T
ENST00000703101.1:c.295G>T	ENSP00000515169.1:p.Ala99Ser
ENST00000369329.8:c.1531G>T MANE Select	ENSP00000358335.3:p.Ala511Ser
ENST00000369320.1:c.493G>T	ENSP00000358326.1:p.Ala165Ser
ENST00000369325.7:c.1524+702G>T	ENSP00000358331.3:n.1524+702G>T
ENST00000369327.7:c.1443+702G>T	ENSP00000358333.3:n.1443+702G>T
ENST00000369329.7:c.1531G>T	ENSP00000358335.3:p.Ala511Ser
ENST00000369332.7:c.1450G>T	ENSP00000358338.3:p.Ala484Ser
ENST00000479630.1:n.1057G>T
NM_003188.3:c.1450G>T	NP_003179.1:p.Ala484Ser
NM_145331.2:c.1531G>T	NP_663304.1:p.Ala511Ser
NM_145332.2:c.1524+702G>T	NP_663305.1:n.1524+702G>T
NM_145333.2:c.1443+702G>T	NP_663306.1:n.1443+702G>T
XM_006715553.2:c.1141G>T	XP_006715616.1:p.Ala381Ser
XM_006715553.3:c.1141G>T	XP_006715616.1:p.Ala381Ser
XM_017011226.2:c.1060G>T	XP_016866715.1:p.Ala354Ser
NM_145331.3:c.1531G>T MANE Select	NP_663304.1:p.Ala511Ser
NM_003188.4:c.1450G>T	NP_003179.1:p.Ala484Ser
NM_145332.3:c.1524+702G>T	NP_663305.1:n.1524+702G>T
NM_145333.3:c.1443+702G>T	NP_663306.1:n.1443+702G>T