Canonical Allele Identifier: CA381148838

Gene: MAP4K2

Linked Data

• MyVariant Identifiers: chr11:g.64557058T>A (hg19) ; chr11:g.64789586T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2414A>T MANE Select	ENSP00000294066.2:p.Glu805Val
ENST00000294066.6:c.2414A>T	ENSP00000294066.2:p.Glu805Val
ENST00000377350.7:c.2390A>T	ENSP00000366567.3:p.Glu797Val
ENST00000424945.5:c.726A>T
ENST00000433890.5:c.2361A>T	ENSP00000413167.1:n.2361A>T
ENST00000435926.5:c.*2214A>T	ENSP00000400594.1:n.*2214A>T
ENST00000470088.5:n.1356A>T
NM_001307990.1:c.2390A>T	NP_001294919.1:p.Glu797Val
NM_004579.3:c.2414A>T	NP_004570.2:p.Glu805Val
NM_004579.4:c.2414A>T	NP_004570.2:p.Glu805Val
XM_011545202.1:c.2390A>T	XP_011543504.1:p.Glu797Val
XM_011545203.1:c.2345A>T	XP_011543505.1:p.Glu782Val
XM_011545204.1:c.2282A>T	XP_011543506.1:p.Glu761Val
XM_011545204.3:c.2282A>T	XP_011543506.1:p.Glu761Val
XM_017018093.2:c.2258A>T	XP_016873582.1:p.Glu753Val
XM_017018095.2:c.1814A>T	XP_016873584.1:p.Glu605Val
XM_024448629.1:c.2534A>T	XP_024304397.1:p.Glu845Val
XM_024448630.1:c.2465A>T	XP_024304398.1:p.Glu822Val
XM_024448631.1:c.2402A>T	XP_024304399.1:p.Glu801Val
XM_024448633.1:c.2003A>T	XP_024304401.1:p.Glu668Val
XR_002957155.1:n.2628A>T
NM_004579.5:c.2414A>T MANE Select	NP_004570.2:p.Glu805Val
NM_001307990.2:c.2390A>T	NP_001294919.1:p.Glu797Val