Canonical Allele Identifier: CA381148912

Gene: MAP4K2

Linked Data

• MyVariant Identifiers: chr11:g.64557068C>A (hg19) ; chr11:g.64789596C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64789596C>A , CM000673.2:g.64789596C>A	GRCh38
NC_000011.9:g.64557068C>A , CM000673.1:g.64557068C>A	GRCh37
NC_000011.8:g.64313644C>A	NCBI36
NG_033040.1:g.18646G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2404G>T MANE Select	ENSP00000294066.2:p.Asp802Tyr
ENST00000294066.6:c.2404G>T	ENSP00000294066.2:p.Asp802Tyr
ENST00000377350.7:c.2380G>T	ENSP00000366567.3:p.Asp794Tyr
ENST00000424945.5:c.716G>T
ENST00000433890.5:c.2351G>T	ENSP00000413167.1:n.2351G>T
ENST00000435926.5:c.*2204G>T	ENSP00000400594.1:n.*2204G>T
ENST00000470088.5:n.1346G>T
NM_001307990.1:c.2380G>T	NP_001294919.1:p.Asp794Tyr
NM_004579.3:c.2404G>T	NP_004570.2:p.Asp802Tyr
NM_004579.4:c.2404G>T	NP_004570.2:p.Asp802Tyr
XM_011545202.1:c.2380G>T	XP_011543504.1:p.Asp794Tyr
XM_011545203.1:c.2335G>T	XP_011543505.1:p.Asp779Tyr
XM_011545204.1:c.2272G>T	XP_011543506.1:p.Asp758Tyr
XM_011545204.3:c.2272G>T	XP_011543506.1:p.Asp758Tyr
XM_017018093.2:c.2248G>T	XP_016873582.1:p.Asp750Tyr
XM_017018095.2:c.1804G>T	XP_016873584.1:p.Asp602Tyr
XM_024448629.1:c.2524G>T	XP_024304397.1:p.Asp842Tyr
XM_024448630.1:c.2455G>T	XP_024304398.1:p.Asp819Tyr
XM_024448631.1:c.2392G>T	XP_024304399.1:p.Asp798Tyr
XM_024448633.1:c.1993G>T	XP_024304401.1:p.Asp665Tyr
XR_002957155.1:n.2618G>T
NM_004579.5:c.2404G>T MANE Select	NP_004570.2:p.Asp802Tyr
NM_001307990.2:c.2380G>T	NP_001294919.1:p.Asp794Tyr