Canonical Allele Identifier: CA5459695

Gene: MAP3K8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30450326A>G , CM000672.2:g.30450326A>G	GRCh38
NC_000010.10:g.30739255A>G , CM000672.1:g.30739255A>G	GRCh37
NC_000010.9:g.30779261A>G	NCBI36
NG_029984.1:g.21306A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263056.6:c.573A>G MANE Select	ENSP00000263056.1:p.Ala191=
ENST00000263056.5:c.573A>G	ENSP00000263056.1:p.Ala191=
ENST00000375321.1:c.573A>G	ENSP00000364470.1:p.Ala191=
ENST00000413724.5:c.573A>G	ENSP00000391275.1:p.Ala191=
ENST00000415139.5:c.573A>G	ENSP00000409653.1:p.Ala191=
ENST00000430603.1:n.335A>G
ENST00000542547.5:c.573A>G	ENSP00000443610.1:p.Ala191=
NM_001244134.1:c.573A>G	NP_001231063.1:p.Ala191=
NM_005204.3:c.573A>G	NP_005195.2:p.Ala191=
XM_005252364.2:c.573A>G	XP_005252421.2:p.Ala191=
XM_011519308.1:c.954A>G	XP_011517610.1:p.Ala318=
XM_011519309.1:c.660A>G	XP_011517611.1:p.Ala220=
XM_011519310.1:c.639A>G	XP_011517612.1:p.Ala213=
XM_011519311.1:c.639A>G	XP_011517613.1:p.Ala213=
XM_011519312.1:c.639A>G	XP_011517614.1:p.Ala213=
XM_011519313.1:c.639A>G	XP_011517615.1:p.Ala213=
XM_011519314.1:c.639A>G	XP_011517616.1:p.Ala213=
XM_011519315.1:c.639A>G	XP_011517617.1:p.Ala213=
NM_001320961.1:c.573A>G	NP_001307890.1:p.Ala191=
XM_017015708.1:c.573A>G	XP_016871197.1:p.Ala191=
XM_017015709.2:c.573A>G	XP_016871198.1:p.Ala191=
XM_017015710.1:c.573A>G	XP_016871199.1:p.Ala191=
XM_017015711.2:c.84A>G	XP_016871200.1:p.Ala28=
XM_017015712.1:c.84A>G	XP_016871201.1:p.Ala28=
XM_017015713.1:c.84A>G	XP_016871202.1:p.Ala28=
XM_017015714.1:c.84A>G	XP_016871203.1:p.Ala28=
XM_024447819.1:c.84A>G	XP_024303587.1:p.Ala28=
NM_005204.4:c.573A>G MANE Select	NP_005195.2:p.Ala191=
NM_001320961.2:c.573A>G	NP_001307890.1:p.Ala191=