Canonical Allele Identifier: CA381148814

Gene: MAP4K2

Linked Data

• gnomAD v4: 11-64789583-G-T
• MyVariant Identifiers: chr11:g.64557055G>T (hg19) ; chr11:g.64789583G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64789583G>T , CM000673.2:g.64789583G>T	GRCh38
NC_000011.9:g.64557055G>T , CM000673.1:g.64557055G>T	GRCh37
NC_000011.8:g.64313631G>T	NCBI36
NG_033040.1:g.18659C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2417C>A MANE Select	ENSP00000294066.2:p.Ala806Glu
ENST00000294066.6:c.2417C>A	ENSP00000294066.2:p.Ala806Glu
ENST00000377350.7:c.2393C>A	ENSP00000366567.3:p.Ala798Glu
ENST00000424945.5:c.729C>A
ENST00000433890.5:c.2364C>A	ENSP00000413167.1:n.2364C>A
ENST00000435926.5:c.*2217C>A	ENSP00000400594.1:n.*2217C>A
ENST00000470088.5:n.1359C>A
NM_001307990.1:c.2393C>A	NP_001294919.1:p.Ala798Glu
NM_004579.3:c.2417C>A	NP_004570.2:p.Ala806Glu
NM_004579.4:c.2417C>A	NP_004570.2:p.Ala806Glu
XM_011545202.1:c.2393C>A	XP_011543504.1:p.Ala798Glu
XM_011545203.1:c.2348C>A	XP_011543505.1:p.Ala783Glu
XM_011545204.1:c.2285C>A	XP_011543506.1:p.Ala762Glu
XM_011545204.3:c.2285C>A	XP_011543506.1:p.Ala762Glu
XM_017018093.2:c.2261C>A	XP_016873582.1:p.Ala754Glu
XM_017018095.2:c.1817C>A	XP_016873584.1:p.Ala606Glu
XM_024448629.1:c.2537C>A	XP_024304397.1:p.Ala846Glu
XM_024448630.1:c.2468C>A	XP_024304398.1:p.Ala823Glu
XM_024448631.1:c.2405C>A	XP_024304399.1:p.Ala802Glu
XM_024448633.1:c.2006C>A	XP_024304401.1:p.Ala669Glu
XR_002957155.1:n.2631C>A
NM_004579.5:c.2417C>A MANE Select	NP_004570.2:p.Ala806Glu
NM_001307990.2:c.2393C>A	NP_001294919.1:p.Ala798Glu