Canonical Allele Identifier: CA381148865

Gene: MAP4K2

Linked Data

• MyVariant Identifiers: chr11:g.64557061G>C (hg19) ; chr11:g.64789589G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64789589G>C , CM000673.2:g.64789589G>C	GRCh38
NC_000011.9:g.64557061G>C , CM000673.1:g.64557061G>C	GRCh37
NC_000011.8:g.64313637G>C	NCBI36
NG_033040.1:g.18653C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2411C>G MANE Select	ENSP00000294066.2:p.Pro804Arg
ENST00000294066.6:c.2411C>G	ENSP00000294066.2:p.Pro804Arg
ENST00000377350.7:c.2387C>G	ENSP00000366567.3:p.Pro796Arg
ENST00000424945.5:c.723C>G
ENST00000433890.5:c.2358C>G	ENSP00000413167.1:n.2358C>G
ENST00000435926.5:c.*2211C>G	ENSP00000400594.1:n.*2211C>G
ENST00000470088.5:n.1353C>G
NM_001307990.1:c.2387C>G	NP_001294919.1:p.Pro796Arg
NM_004579.3:c.2411C>G	NP_004570.2:p.Pro804Arg
NM_004579.4:c.2411C>G	NP_004570.2:p.Pro804Arg
XM_011545202.1:c.2387C>G	XP_011543504.1:p.Pro796Arg
XM_011545203.1:c.2342C>G	XP_011543505.1:p.Pro781Arg
XM_011545204.1:c.2279C>G	XP_011543506.1:p.Pro760Arg
XM_011545204.3:c.2279C>G	XP_011543506.1:p.Pro760Arg
XM_017018093.2:c.2255C>G	XP_016873582.1:p.Pro752Arg
XM_017018095.2:c.1811C>G	XP_016873584.1:p.Pro604Arg
XM_024448629.1:c.2531C>G	XP_024304397.1:p.Pro844Arg
XM_024448630.1:c.2462C>G	XP_024304398.1:p.Pro821Arg
XM_024448631.1:c.2399C>G	XP_024304399.1:p.Pro800Arg
XM_024448633.1:c.2000C>G	XP_024304401.1:p.Pro667Arg
XR_002957155.1:n.2625C>G
NM_004579.5:c.2411C>G MANE Select	NP_004570.2:p.Pro804Arg
NM_001307990.2:c.2387C>G	NP_001294919.1:p.Pro796Arg