Canonical Allele Identifier: CA10588011
Community Standard Title: NM_145331.3(MAP3K7):c.328G>T (p.Gly110Cys)
Gene: MAP3K7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.90561637C>A , CM000668.2:g.90561637C>A GRCh38
NC_000006.11:g.91271356C>A , CM000668.1:g.91271356C>A GRCh37
NC_000006.10:g.91328077C>A NCBI36
NG_011966.2:g.30552G>T

Transcript Alleles

HGVS Amino-acid Change
NM_145331.3:c.328G>T MANE Select NP_663304.1:p.Gly110Cys
ENST00000369329.8:c.328G>T MANE Select ENSP00000358335.3:p.Gly110Cys
NM_003188.3:c.328G>T NP_003179.1:p.Gly110Cys
NM_003188.4:c.328G>T NP_003179.1:p.Gly110Cys
NM_145331.2:c.328G>T NP_663304.1:p.Gly110Cys
NM_145332.2:c.328G>T NP_663305.1:p.Gly110Cys
NM_145332.3:c.328G>T NP_663305.1:p.Gly110Cys
NM_145333.2:c.328G>T NP_663306.1:p.Gly110Cys
NM_145333.3:c.328G>T NP_663306.1:p.Gly110Cys
ENST00000369325.7:c.328G>T ENSP00000358331.3:p.Gly110Cys
ENST00000369327.7:c.328G>T ENSP00000358333.3:p.Gly110Cys
ENST00000369329.7:c.328G>T ENSP00000358335.3:p.Gly110Cys
ENST00000369332.7:c.328G>T ENSP00000358338.3:p.Gly110Cys
ENST00000700580.1:c.328G>T ENSP00000515074.1:p.Gly110Cys
ENST00000700581.1:c.328G>T ENSP00000515075.1:p.Gly110Cys
ENST00000700582.1:c.328G>T ENSP00000515076.1:p.Gly110Cys
ENST00000700583.1:c.328G>T ENSP00000515077.1:p.Gly110Cys
ENST00000700584.1:c.*289G>T ENSP00000515078.1:n.*289G>T
ENST00000700587.1:c.*267G>T ENSP00000515080.1:n.*267G>T
ENST00000700588.1:n.394G>T
ENST00000700589.1:c.328G>T ENSP00000515081.1:p.Gly110Cys
ENST00000700590.1:n.517G>T
ENST00000700591.1:c.262G>T ENSP00000515082.1:p.Gly88Cys
ENST00000700592.1:c.403G>T ENSP00000515083.1:p.Gly135Cys
ENST00000700593.1:c.19G>T ENSP00000515084.1:p.Gly7Cys
ENST00000700594.1:c.*62G>T ENSP00000515085.1:n.*62G>T
ENST00000703100.1:c.328G>T ENSP00000515168.1:p.Gly110Cys
ENST00000703101.1:c.120+25127G>T ENSP00000515169.1:n.120+25127G>T
XM_006715553.2:c.-83G>T XP_006715616.1:n.-83G>T
XM_006715553.3:c.-83G>T XP_006715616.1:n.-83G>T
XM_017011226.2:c.-83G>T XP_016866715.1:n.-83G>T