Canonical Allele Identifier: CA474976868

Gene: MAP4K2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2409C>T MANE Select	ENSP00000294066.2:p.Asn803=
ENST00000294066.6:c.2409C>T	ENSP00000294066.2:p.Asn803=
ENST00000377350.7:c.2385C>T	ENSP00000366567.3:p.Asn795=
ENST00000424945.5:c.721C>T
ENST00000433890.5:c.2356C>T	ENSP00000413167.1:n.2356C>T
ENST00000435926.5:c.*2209C>T	ENSP00000400594.1:n.*2209C>T
ENST00000470088.5:n.1351C>T
NM_001307990.1:c.2385C>T	NP_001294919.1:p.Asn795=
NM_004579.3:c.2409C>T	NP_004570.2:p.Asn803=
NM_004579.4:c.2409C>T	NP_004570.2:p.Asn803=
XM_011545202.1:c.2385C>T	XP_011543504.1:p.Asn795=
XM_011545203.1:c.2340C>T	XP_011543505.1:p.Asn780=
XM_011545204.1:c.2277C>T	XP_011543506.1:p.Asn759=
XM_011545204.3:c.2277C>T	XP_011543506.1:p.Asn759=
XM_017018093.2:c.2253C>T	XP_016873582.1:p.Asn751=
XM_017018095.2:c.1809C>T	XP_016873584.1:p.Asn603=
XM_024448629.1:c.2529C>T	XP_024304397.1:p.Asn843=
XM_024448630.1:c.2460C>T	XP_024304398.1:p.Asn820=
XM_024448631.1:c.2397C>T	XP_024304399.1:p.Asn799=
XM_024448633.1:c.1998C>T	XP_024304401.1:p.Asn666=
XR_002957155.1:n.2623C>T
NM_004579.5:c.2409C>T MANE Select	NP_004570.2:p.Asn803=
NM_001307990.2:c.2385C>T	NP_001294919.1:p.Asn795=