Canonical Allele Identifier: CA381148891

Gene: MAP4K2

Linked Data

• MyVariant Identifiers: chr11:g.64557065T>G (hg19) ; chr11:g.64789593T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64789593T>G , CM000673.2:g.64789593T>G	GRCh38
NC_000011.9:g.64557065T>G , CM000673.1:g.64557065T>G	GRCh37
NC_000011.8:g.64313641T>G	NCBI36
NG_033040.1:g.18649A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294066.7:c.2407A>C MANE Select	ENSP00000294066.2:p.Asn803His
ENST00000294066.6:c.2407A>C	ENSP00000294066.2:p.Asn803His
ENST00000377350.7:c.2383A>C	ENSP00000366567.3:p.Asn795His
ENST00000424945.5:c.719A>C
ENST00000433890.5:c.2354A>C	ENSP00000413167.1:n.2354A>C
ENST00000435926.5:c.*2207A>C	ENSP00000400594.1:n.*2207A>C
ENST00000470088.5:n.1349A>C
NM_001307990.1:c.2383A>C	NP_001294919.1:p.Asn795His
NM_004579.3:c.2407A>C	NP_004570.2:p.Asn803His
NM_004579.4:c.2407A>C	NP_004570.2:p.Asn803His
XM_011545202.1:c.2383A>C	XP_011543504.1:p.Asn795His
XM_011545203.1:c.2338A>C	XP_011543505.1:p.Asn780His
XM_011545204.1:c.2275A>C	XP_011543506.1:p.Asn759His
XM_011545204.3:c.2275A>C	XP_011543506.1:p.Asn759His
XM_017018093.2:c.2251A>C	XP_016873582.1:p.Asn751His
XM_017018095.2:c.1807A>C	XP_016873584.1:p.Asn603His
XM_024448629.1:c.2527A>C	XP_024304397.1:p.Asn843His
XM_024448630.1:c.2458A>C	XP_024304398.1:p.Asn820His
XM_024448631.1:c.2395A>C	XP_024304399.1:p.Asn799His
XM_024448633.1:c.1996A>C	XP_024304401.1:p.Asn666His
XR_002957155.1:n.2621A>C
NM_004579.5:c.2407A>C MANE Select	NP_004570.2:p.Asn803His
NM_001307990.2:c.2383A>C	NP_001294919.1:p.Asn795His