Canonical Allele Identifier: CA381148899

Gene: MAP4K2

Linked Data

• MyVariant Identifiers: chr11:g.64557067T>C (hg19) ; chr11:g.64789595T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64789595T>C , CM000673.2:g.64789595T>C	GRCh38
NC_000011.9:g.64557067T>C , CM000673.1:g.64557067T>C	GRCh37
NC_000011.8:g.64313643T>C	NCBI36
NG_033040.1:g.18647A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2405A>G MANE Select	ENSP00000294066.2:p.Asp802Gly
ENST00000294066.6:c.2405A>G	ENSP00000294066.2:p.Asp802Gly
ENST00000377350.7:c.2381A>G	ENSP00000366567.3:p.Asp794Gly
ENST00000424945.5:c.717A>G
ENST00000433890.5:c.2352A>G	ENSP00000413167.1:n.2352A>G
ENST00000435926.5:c.*2205A>G	ENSP00000400594.1:n.*2205A>G
ENST00000470088.5:n.1347A>G
NM_001307990.1:c.2381A>G	NP_001294919.1:p.Asp794Gly
NM_004579.3:c.2405A>G	NP_004570.2:p.Asp802Gly
NM_004579.4:c.2405A>G	NP_004570.2:p.Asp802Gly
XM_011545202.1:c.2381A>G	XP_011543504.1:p.Asp794Gly
XM_011545203.1:c.2336A>G	XP_011543505.1:p.Asp779Gly
XM_011545204.1:c.2273A>G	XP_011543506.1:p.Asp758Gly
XM_011545204.3:c.2273A>G	XP_011543506.1:p.Asp758Gly
XM_017018093.2:c.2249A>G	XP_016873582.1:p.Asp750Gly
XM_017018095.2:c.1805A>G	XP_016873584.1:p.Asp602Gly
XM_024448629.1:c.2525A>G	XP_024304397.1:p.Asp842Gly
XM_024448630.1:c.2456A>G	XP_024304398.1:p.Asp819Gly
XM_024448631.1:c.2393A>G	XP_024304399.1:p.Asp798Gly
XM_024448633.1:c.1994A>G	XP_024304401.1:p.Asp665Gly
XR_002957155.1:n.2619A>G
NM_004579.5:c.2405A>G MANE Select	NP_004570.2:p.Asp802Gly
NM_001307990.2:c.2381A>G	NP_001294919.1:p.Asp794Gly