Canonical Allele Identifier: CA474976867

Gene: MAP4K2

Linked Data

• gnomAD v4: 11-64789588-T-C
• MyVariant Identifiers: chr11:g.64557060T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64789588T>C , CM000673.2:g.64789588T>C	GRCh38
NC_000011.9:g.64557060T>C , CM000673.1:g.64557060T>C	GRCh37
NC_000011.8:g.64313636T>C	NCBI36
NG_033040.1:g.18654A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2412A>G MANE Select	ENSP00000294066.2:p.Pro804=
ENST00000294066.6:c.2412A>G	ENSP00000294066.2:p.Pro804=
ENST00000377350.7:c.2388A>G	ENSP00000366567.3:p.Pro796=
ENST00000424945.5:c.724A>G
ENST00000433890.5:c.2359A>G	ENSP00000413167.1:n.2359A>G
ENST00000435926.5:c.*2212A>G	ENSP00000400594.1:n.*2212A>G
ENST00000470088.5:n.1354A>G
NM_001307990.1:c.2388A>G	NP_001294919.1:p.Pro796=
NM_004579.3:c.2412A>G	NP_004570.2:p.Pro804=
NM_004579.4:c.2412A>G	NP_004570.2:p.Pro804=
XM_011545202.1:c.2388A>G	XP_011543504.1:p.Pro796=
XM_011545203.1:c.2343A>G	XP_011543505.1:p.Pro781=
XM_011545204.1:c.2280A>G	XP_011543506.1:p.Pro760=
XM_011545204.3:c.2280A>G	XP_011543506.1:p.Pro760=
XM_017018093.2:c.2256A>G	XP_016873582.1:p.Pro752=
XM_017018095.2:c.1812A>G	XP_016873584.1:p.Pro604=
XM_024448629.1:c.2532A>G	XP_024304397.1:p.Pro844=
XM_024448630.1:c.2463A>G	XP_024304398.1:p.Pro821=
XM_024448631.1:c.2400A>G	XP_024304399.1:p.Pro800=
XM_024448633.1:c.2001A>G	XP_024304401.1:p.Pro667=
XR_002957155.1:n.2626A>G
NM_004579.5:c.2412A>G MANE Select	NP_004570.2:p.Pro804=
NM_001307990.2:c.2388A>G	NP_001294919.1:p.Pro796=