Canonical Allele Identifier: CA381148845

Gene: MAP4K2

Linked Data

• gnomAD v4: 11-64789586-T-C
• MyVariant Identifiers: chr11:g.64557058T>C (hg19) ; chr11:g.64789586T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64789586T>C , CM000673.2:g.64789586T>C	GRCh38
NC_000011.9:g.64557058T>C , CM000673.1:g.64557058T>C	GRCh37
NC_000011.8:g.64313634T>C	NCBI36
NG_033040.1:g.18656A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2414A>G MANE Select	ENSP00000294066.2:p.Glu805Gly
ENST00000294066.6:c.2414A>G	ENSP00000294066.2:p.Glu805Gly
ENST00000377350.7:c.2390A>G	ENSP00000366567.3:p.Glu797Gly
ENST00000424945.5:c.726A>G
ENST00000433890.5:c.2361A>G	ENSP00000413167.1:n.2361A>G
ENST00000435926.5:c.*2214A>G	ENSP00000400594.1:n.*2214A>G
ENST00000470088.5:n.1356A>G
NM_001307990.1:c.2390A>G	NP_001294919.1:p.Glu797Gly
NM_004579.3:c.2414A>G	NP_004570.2:p.Glu805Gly
NM_004579.4:c.2414A>G	NP_004570.2:p.Glu805Gly
XM_011545202.1:c.2390A>G	XP_011543504.1:p.Glu797Gly
XM_011545203.1:c.2345A>G	XP_011543505.1:p.Glu782Gly
XM_011545204.1:c.2282A>G	XP_011543506.1:p.Glu761Gly
XM_011545204.3:c.2282A>G	XP_011543506.1:p.Glu761Gly
XM_017018093.2:c.2258A>G	XP_016873582.1:p.Glu753Gly
XM_017018095.2:c.1814A>G	XP_016873584.1:p.Glu605Gly
XM_024448629.1:c.2534A>G	XP_024304397.1:p.Glu845Gly
XM_024448630.1:c.2465A>G	XP_024304398.1:p.Glu822Gly
XM_024448631.1:c.2402A>G	XP_024304399.1:p.Glu801Gly
XM_024448633.1:c.2003A>G	XP_024304401.1:p.Glu668Gly
XR_002957155.1:n.2628A>G
NM_004579.5:c.2414A>G MANE Select	NP_004570.2:p.Glu805Gly
NM_001307990.2:c.2390A>G	NP_001294919.1:p.Glu797Gly