Canonical Allele Identifier: CA1899373136

Gene: MAP3K8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30439297G= , CM000672.2:g.30439297G=	GRCh38
NC_000010.10:g.30728226G= , CM000672.1:g.30728226G=	GRCh37
NC_000010.9:g.30768232G=	NCBI36
NG_029984.1:g.10277G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263056.6:c.336+23G= MANE Select	ENSP00000263056.1:n.336+23G=
ENST00000263056.5:c.336+23G=	ENSP00000263056.1:n.336+23G=
ENST00000375321.1:c.336+23G=	ENSP00000364470.1:n.336+23G=
ENST00000375322.2:c.359G=	ENSP00000364471.1:p.Trp120=
ENST00000413724.5:c.336+23G=	ENSP00000391275.1:n.336+23G=
ENST00000415139.5:c.336+23G=	ENSP00000409653.1:n.336+23G=
ENST00000430603.1:n.98+23G=
ENST00000542547.5:c.336+23G=	ENSP00000443610.1:n.336+23G=
NM_001244134.1:c.336+23G=	NP_001231063.1:n.336+23G=
NM_005204.3:c.336+23G=	NP_005195.2:n.336+23G=
XM_005252364.2:c.336+23G=	XP_005252421.2:n.336+23G=
XM_011519308.1:c.651+23G=	XP_011517610.1:n.651+23G=
XM_011519309.1:c.423+4549G=	XP_011517611.1:n.423+4549G=
XM_011519310.1:c.336+23G=	XP_011517612.1:n.336+23G=
XM_011519311.1:c.336+23G=	XP_011517613.1:n.336+23G=
XM_011519312.1:c.336+23G=	XP_011517614.1:n.336+23G=
XM_011519313.1:c.336+23G=	XP_011517615.1:n.336+23G=
XM_011519314.1:c.336+23G=	XP_011517616.1:n.336+23G=
XM_011519315.1:c.336+23G=	XP_011517617.1:n.336+23G=
NM_001320961.1:c.336+23G=	NP_001307890.1:n.336+23G=
XM_017015708.1:c.336+23G=	XP_016871197.1:n.336+23G=
XM_017015709.2:c.336+23G=	XP_016871198.1:n.336+23G=
XM_017015710.1:c.336+23G=	XP_016871199.1:n.336+23G=
XM_017015711.2:c.-3493G=	XP_016871200.1:n.-3493G=
XM_017015712.1:c.-3493G=	XP_016871201.1:n.-3493G=
XM_017015713.1:c.-3493G=	XP_016871202.1:n.-3493G=
XM_017015714.1:c.-3493G=	XP_016871203.1:n.-3493G=
XM_024447819.1:c.-3493G=	XP_024303587.1:n.-3493G=
NM_005204.4:c.336+23G= MANE Select	NP_005195.2:n.336+23G=
NM_001320961.2:c.336+23G=	NP_001307890.1:n.336+23G=