Canonical Allele Identifier: CA1978888814

Gene: MAP4K2

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2408A= MANE Select	ENSP00000294066.2:p.Asn803=
ENST00000294066.6:c.2408A=	ENSP00000294066.2:p.Asn803=
ENST00000377350.7:c.2384A=	ENSP00000366567.3:p.Asn795=
ENST00000424945.5:c.720A=
ENST00000433890.5:c.2355A=	ENSP00000413167.1:n.2355A=
ENST00000435926.5:c.*2208A=	ENSP00000400594.1:n.*2208A=
ENST00000470088.5:n.1350A=
NM_001307990.1:c.2384A=	NP_001294919.1:p.Asn795=
NM_004579.3:c.2408A=	NP_004570.2:p.Asn803=
NM_004579.4:c.2408A=	NP_004570.2:p.Asn803=
XM_011545202.1:c.2384A=	XP_011543504.1:p.Asn795=
XM_011545203.1:c.2339A=	XP_011543505.1:p.Asn780=
XM_011545204.1:c.2276A=	XP_011543506.1:p.Asn759=
XM_011545204.3:c.2276A=	XP_011543506.1:p.Asn759=
XM_017018093.2:c.2252A=	XP_016873582.1:p.Asn751=
XM_017018095.2:c.1808A=	XP_016873584.1:p.Asn603=
XM_024448629.1:c.2528A=	XP_024304397.1:p.Asn843=
XM_024448630.1:c.2459A=	XP_024304398.1:p.Asn820=
XM_024448631.1:c.2396A=	XP_024304399.1:p.Asn799=
XM_024448633.1:c.1997A=	XP_024304401.1:p.Asn666=
XR_002957155.1:n.2622A=
NM_004579.5:c.2408A= MANE Select	NP_004570.2:p.Asn803=
NM_001307990.2:c.2384A=	NP_001294919.1:p.Asn795=