Canonical Allele Identifier: CA474976864

Gene: MAP4K2

Linked Data

• MyVariant Identifiers: chr11:g.64557054C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64789582C>G , CM000673.2:g.64789582C>G	GRCh38
NC_000011.9:g.64557054C>G , CM000673.1:g.64557054C>G	GRCh37
NC_000011.8:g.64313630C>G	NCBI36
NG_033040.1:g.18660G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2418G>C MANE Select	ENSP00000294066.2:p.Ala806=
ENST00000294066.6:c.2418G>C	ENSP00000294066.2:p.Ala806=
ENST00000377350.7:c.2394G>C	ENSP00000366567.3:p.Ala798=
ENST00000424945.5:c.730G>C
ENST00000433890.5:c.2365G>C	ENSP00000413167.1:n.2365G>C
ENST00000435926.5:c.*2218G>C	ENSP00000400594.1:n.*2218G>C
ENST00000470088.5:n.1360G>C
NM_001307990.1:c.2394G>C	NP_001294919.1:p.Ala798=
NM_004579.3:c.2418G>C	NP_004570.2:p.Ala806=
NM_004579.4:c.2418G>C	NP_004570.2:p.Ala806=
XM_011545202.1:c.2394G>C	XP_011543504.1:p.Ala798=
XM_011545203.1:c.2349G>C	XP_011543505.1:p.Ala783=
XM_011545204.1:c.2286G>C	XP_011543506.1:p.Ala762=
XM_011545204.3:c.2286G>C	XP_011543506.1:p.Ala762=
XM_017018093.2:c.2262G>C	XP_016873582.1:p.Ala754=
XM_017018095.2:c.1818G>C	XP_016873584.1:p.Ala606=
XM_024448629.1:c.2538G>C	XP_024304397.1:p.Ala846=
XM_024448630.1:c.2469G>C	XP_024304398.1:p.Ala823=
XM_024448631.1:c.2406G>C	XP_024304399.1:p.Ala802=
XM_024448633.1:c.2007G>C	XP_024304401.1:p.Ala669=
XR_002957155.1:n.2632G>C
NM_004579.5:c.2418G>C MANE Select	NP_004570.2:p.Ala806=
NM_001307990.2:c.2394G>C	NP_001294919.1:p.Ala798=