Canonical Allele Identifier: CA381148886

Gene: MAP4K2

Linked Data

• dbSNP Id: rs1277359749
• gnomAD v3: 11-64789592-T-C
• gnomAD v4: 11-64789592-T-C
• MyVariant Identifiers: chr11:g.64557064T>C (hg19) ; chr11:g.64789592T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64789592T>C , CM000673.2:g.64789592T>C	GRCh38
NC_000011.9:g.64557064T>C , CM000673.1:g.64557064T>C	GRCh37
NC_000011.8:g.64313640T>C	NCBI36
NG_033040.1:g.18650A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2408A>G MANE Select	ENSP00000294066.2:p.Asn803Ser
ENST00000294066.6:c.2408A>G	ENSP00000294066.2:p.Asn803Ser
ENST00000377350.7:c.2384A>G	ENSP00000366567.3:p.Asn795Ser
ENST00000424945.5:c.720A>G
ENST00000433890.5:c.2355A>G	ENSP00000413167.1:n.2355A>G
ENST00000435926.5:c.*2208A>G	ENSP00000400594.1:n.*2208A>G
ENST00000470088.5:n.1350A>G
NM_001307990.1:c.2384A>G	NP_001294919.1:p.Asn795Ser
NM_004579.3:c.2408A>G	NP_004570.2:p.Asn803Ser
NM_004579.4:c.2408A>G	NP_004570.2:p.Asn803Ser
XM_011545202.1:c.2384A>G	XP_011543504.1:p.Asn795Ser
XM_011545203.1:c.2339A>G	XP_011543505.1:p.Asn780Ser
XM_011545204.1:c.2276A>G	XP_011543506.1:p.Asn759Ser
XM_011545204.3:c.2276A>G	XP_011543506.1:p.Asn759Ser
XM_017018093.2:c.2252A>G	XP_016873582.1:p.Asn751Ser
XM_017018095.2:c.1808A>G	XP_016873584.1:p.Asn603Ser
XM_024448629.1:c.2528A>G	XP_024304397.1:p.Asn843Ser
XM_024448630.1:c.2459A>G	XP_024304398.1:p.Asn820Ser
XM_024448631.1:c.2396A>G	XP_024304399.1:p.Asn799Ser
XM_024448633.1:c.1997A>G	XP_024304401.1:p.Asn666Ser
XR_002957155.1:n.2622A>G
NM_004579.5:c.2408A>G MANE Select	NP_004570.2:p.Asn803Ser
NM_001307990.2:c.2384A>G	NP_001294919.1:p.Asn795Ser