Canonical Allele Identifier: CA381148885

Gene: MAP4K2

Linked Data

• MyVariant Identifiers: chr11:g.64557064T>G (hg19) ; chr11:g.64789592T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2408A>C MANE Select	ENSP00000294066.2:p.Asn803Thr
ENST00000294066.6:c.2408A>C	ENSP00000294066.2:p.Asn803Thr
ENST00000377350.7:c.2384A>C	ENSP00000366567.3:p.Asn795Thr
ENST00000424945.5:c.720A>C
ENST00000433890.5:c.2355A>C	ENSP00000413167.1:n.2355A>C
ENST00000435926.5:c.*2208A>C	ENSP00000400594.1:n.*2208A>C
ENST00000470088.5:n.1350A>C
NM_001307990.1:c.2384A>C	NP_001294919.1:p.Asn795Thr
NM_004579.3:c.2408A>C	NP_004570.2:p.Asn803Thr
NM_004579.4:c.2408A>C	NP_004570.2:p.Asn803Thr
XM_011545202.1:c.2384A>C	XP_011543504.1:p.Asn795Thr
XM_011545203.1:c.2339A>C	XP_011543505.1:p.Asn780Thr
XM_011545204.1:c.2276A>C	XP_011543506.1:p.Asn759Thr
XM_011545204.3:c.2276A>C	XP_011543506.1:p.Asn759Thr
XM_017018093.2:c.2252A>C	XP_016873582.1:p.Asn751Thr
XM_017018095.2:c.1808A>C	XP_016873584.1:p.Asn603Thr
XM_024448629.1:c.2528A>C	XP_024304397.1:p.Asn843Thr
XM_024448630.1:c.2459A>C	XP_024304398.1:p.Asn820Thr
XM_024448631.1:c.2396A>C	XP_024304399.1:p.Asn799Thr
XM_024448633.1:c.1997A>C	XP_024304401.1:p.Asn666Thr
XR_002957155.1:n.2622A>C
NM_004579.5:c.2408A>C MANE Select	NP_004570.2:p.Asn803Thr
NM_001307990.2:c.2384A>C	NP_001294919.1:p.Asn795Thr