Canonical Allele Identifier: CA381148871

Gene: MAP4K2

Linked Data

• gnomAD v4: 11-64789591-G-C
• MyVariant Identifiers: chr11:g.64557063G>C (hg19) ; chr11:g.64789591G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64789591G>C , CM000673.2:g.64789591G>C	GRCh38
NC_000011.9:g.64557063G>C , CM000673.1:g.64557063G>C	GRCh37
NC_000011.8:g.64313639G>C	NCBI36
NG_033040.1:g.18651C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2409C>G MANE Select	ENSP00000294066.2:p.Asn803Lys
ENST00000294066.6:c.2409C>G	ENSP00000294066.2:p.Asn803Lys
ENST00000377350.7:c.2385C>G	ENSP00000366567.3:p.Asn795Lys
ENST00000424945.5:c.721C>G
ENST00000433890.5:c.2356C>G	ENSP00000413167.1:n.2356C>G
ENST00000435926.5:c.*2209C>G	ENSP00000400594.1:n.*2209C>G
ENST00000470088.5:n.1351C>G
NM_001307990.1:c.2385C>G	NP_001294919.1:p.Asn795Lys
NM_004579.3:c.2409C>G	NP_004570.2:p.Asn803Lys
NM_004579.4:c.2409C>G	NP_004570.2:p.Asn803Lys
XM_011545202.1:c.2385C>G	XP_011543504.1:p.Asn795Lys
XM_011545203.1:c.2340C>G	XP_011543505.1:p.Asn780Lys
XM_011545204.1:c.2277C>G	XP_011543506.1:p.Asn759Lys
XM_011545204.3:c.2277C>G	XP_011543506.1:p.Asn759Lys
XM_017018093.2:c.2253C>G	XP_016873582.1:p.Asn751Lys
XM_017018095.2:c.1809C>G	XP_016873584.1:p.Asn603Lys
XM_024448629.1:c.2529C>G	XP_024304397.1:p.Asn843Lys
XM_024448630.1:c.2460C>G	XP_024304398.1:p.Asn820Lys
XM_024448631.1:c.2397C>G	XP_024304399.1:p.Asn799Lys
XM_024448633.1:c.1998C>G	XP_024304401.1:p.Asn666Lys
XR_002957155.1:n.2623C>G
NM_004579.5:c.2409C>G MANE Select	NP_004570.2:p.Asn803Lys
NM_001307990.2:c.2385C>G	NP_001294919.1:p.Asn795Lys