Canonical Allele Identifier: CA381148870

Gene: MAP4K2

Linked Data

• MyVariant Identifiers: chr11:g.64557062G>T (hg19) ; chr11:g.64789590G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64789590G>T , CM000673.2:g.64789590G>T	GRCh38
NC_000011.9:g.64557062G>T , CM000673.1:g.64557062G>T	GRCh37
NC_000011.8:g.64313638G>T	NCBI36
NG_033040.1:g.18652C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2410C>A MANE Select	ENSP00000294066.2:p.Pro804Thr
ENST00000294066.6:c.2410C>A	ENSP00000294066.2:p.Pro804Thr
ENST00000377350.7:c.2386C>A	ENSP00000366567.3:p.Pro796Thr
ENST00000424945.5:c.722C>A
ENST00000433890.5:c.2357C>A	ENSP00000413167.1:n.2357C>A
ENST00000435926.5:c.*2210C>A	ENSP00000400594.1:n.*2210C>A
ENST00000470088.5:n.1352C>A
NM_001307990.1:c.2386C>A	NP_001294919.1:p.Pro796Thr
NM_004579.3:c.2410C>A	NP_004570.2:p.Pro804Thr
NM_004579.4:c.2410C>A	NP_004570.2:p.Pro804Thr
XM_011545202.1:c.2386C>A	XP_011543504.1:p.Pro796Thr
XM_011545203.1:c.2341C>A	XP_011543505.1:p.Pro781Thr
XM_011545204.1:c.2278C>A	XP_011543506.1:p.Pro760Thr
XM_011545204.3:c.2278C>A	XP_011543506.1:p.Pro760Thr
XM_017018093.2:c.2254C>A	XP_016873582.1:p.Pro752Thr
XM_017018095.2:c.1810C>A	XP_016873584.1:p.Pro604Thr
XM_024448629.1:c.2530C>A	XP_024304397.1:p.Pro844Thr
XM_024448630.1:c.2461C>A	XP_024304398.1:p.Pro821Thr
XM_024448631.1:c.2398C>A	XP_024304399.1:p.Pro800Thr
XM_024448633.1:c.1999C>A	XP_024304401.1:p.Pro667Thr
XR_002957155.1:n.2624C>A
NM_004579.5:c.2410C>A MANE Select	NP_004570.2:p.Pro804Thr
NM_001307990.2:c.2386C>A	NP_001294919.1:p.Pro796Thr