Canonical Allele Identifier: CA381148898

Gene: MAP4K2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2405A>T MANE Select	ENSP00000294066.2:p.Asp802Val
ENST00000294066.6:c.2405A>T	ENSP00000294066.2:p.Asp802Val
ENST00000377350.7:c.2381A>T	ENSP00000366567.3:p.Asp794Val
ENST00000424945.5:c.717A>T
ENST00000433890.5:c.2352A>T	ENSP00000413167.1:n.2352A>T
ENST00000435926.5:c.*2205A>T	ENSP00000400594.1:n.*2205A>T
ENST00000470088.5:n.1347A>T
NM_001307990.1:c.2381A>T	NP_001294919.1:p.Asp794Val
NM_004579.3:c.2405A>T	NP_004570.2:p.Asp802Val
NM_004579.4:c.2405A>T	NP_004570.2:p.Asp802Val
XM_011545202.1:c.2381A>T	XP_011543504.1:p.Asp794Val
XM_011545203.1:c.2336A>T	XP_011543505.1:p.Asp779Val
XM_011545204.1:c.2273A>T	XP_011543506.1:p.Asp758Val
XM_011545204.3:c.2273A>T	XP_011543506.1:p.Asp758Val
XM_017018093.2:c.2249A>T	XP_016873582.1:p.Asp750Val
XM_017018095.2:c.1805A>T	XP_016873584.1:p.Asp602Val
XM_024448629.1:c.2525A>T	XP_024304397.1:p.Asp842Val
XM_024448630.1:c.2456A>T	XP_024304398.1:p.Asp819Val
XM_024448631.1:c.2393A>T	XP_024304399.1:p.Asp798Val
XM_024448633.1:c.1994A>T	XP_024304401.1:p.Asp665Val
XR_002957155.1:n.2619A>T
NM_004579.5:c.2405A>T MANE Select	NP_004570.2:p.Asp802Val
NM_001307990.2:c.2381A>T	NP_001294919.1:p.Asp794Val