Canonical Allele Identifier: CA381148857

Gene: MAP4K2

Linked Data

• dbSNP Id: rs1940350567
• gnomAD v3: 11-64789587-C-T
• gnomAD v4: 11-64789587-C-T
• MyVariant Identifiers: chr11:g.64557059C>T (hg19) ; chr11:g.64789587C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64789587C>T , CM000673.2:g.64789587C>T	GRCh38
NC_000011.9:g.64557059C>T , CM000673.1:g.64557059C>T	GRCh37
NC_000011.8:g.64313635C>T	NCBI36
NG_033040.1:g.18655G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2413G>A MANE Select	ENSP00000294066.2:p.Glu805Lys
ENST00000294066.6:c.2413G>A	ENSP00000294066.2:p.Glu805Lys
ENST00000377350.7:c.2389G>A	ENSP00000366567.3:p.Glu797Lys
ENST00000424945.5:c.725G>A
ENST00000433890.5:c.2360G>A	ENSP00000413167.1:n.2360G>A
ENST00000435926.5:c.*2213G>A	ENSP00000400594.1:n.*2213G>A
ENST00000470088.5:n.1355G>A
NM_001307990.1:c.2389G>A	NP_001294919.1:p.Glu797Lys
NM_004579.3:c.2413G>A	NP_004570.2:p.Glu805Lys
NM_004579.4:c.2413G>A	NP_004570.2:p.Glu805Lys
XM_011545202.1:c.2389G>A	XP_011543504.1:p.Glu797Lys
XM_011545203.1:c.2344G>A	XP_011543505.1:p.Glu782Lys
XM_011545204.1:c.2281G>A	XP_011543506.1:p.Glu761Lys
XM_011545204.3:c.2281G>A	XP_011543506.1:p.Glu761Lys
XM_017018093.2:c.2257G>A	XP_016873582.1:p.Glu753Lys
XM_017018095.2:c.1813G>A	XP_016873584.1:p.Glu605Lys
XM_024448629.1:c.2533G>A	XP_024304397.1:p.Glu845Lys
XM_024448630.1:c.2464G>A	XP_024304398.1:p.Glu822Lys
XM_024448631.1:c.2401G>A	XP_024304399.1:p.Glu801Lys
XM_024448633.1:c.2002G>A	XP_024304401.1:p.Glu668Lys
XR_002957155.1:n.2627G>A
NM_004579.5:c.2413G>A MANE Select	NP_004570.2:p.Glu805Lys
NM_001307990.2:c.2389G>A	NP_001294919.1:p.Glu797Lys