Canonical Allele Identifier: CA376435626

Gene: MAP3K8

Linked Data

• MyVariant Identifiers: chr10:g.30728006A>G (hg19) ; chr10:g.30439077A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30439077A>G , CM000672.2:g.30439077A>G	GRCh38
NC_000010.10:g.30728006A>G , CM000672.1:g.30728006A>G	GRCh37
NC_000010.9:g.30768012A>G	NCBI36
NG_029984.1:g.10057A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263056.6:c.139A>G MANE Select	ENSP00000263056.1:p.Met47Val
ENST00000263056.5:c.139A>G	ENSP00000263056.1:p.Met47Val
ENST00000375321.1:c.139A>G	ENSP00000364470.1:p.Met47Val
ENST00000375322.2:c.139A>G	ENSP00000364471.1:p.Met47Val
ENST00000413724.5:c.139A>G	ENSP00000391275.1:p.Met47Val
ENST00000415139.5:c.139A>G	ENSP00000409653.1:p.Met47Val
ENST00000542547.5:c.139A>G	ENSP00000443610.1:p.Met47Val
NM_001244134.1:c.139A>G	NP_001231063.1:p.Met47Val
NM_005204.3:c.139A>G	NP_005195.2:p.Met47Val
XM_005252364.2:c.139A>G	XP_005252421.2:p.Met47Val
XM_011519308.1:c.454A>G	XP_011517610.1:p.Met152Val
XM_011519309.1:c.423+4329A>G	XP_011517611.1:n.423+4329A>G
XM_011519310.1:c.139A>G	XP_011517612.1:p.Met47Val
XM_011519311.1:c.139A>G	XP_011517613.1:p.Met47Val
XM_011519312.1:c.139A>G	XP_011517614.1:p.Met47Val
XM_011519313.1:c.139A>G	XP_011517615.1:p.Met47Val
XM_011519314.1:c.139A>G	XP_011517616.1:p.Met47Val
XM_011519315.1:c.139A>G	XP_011517617.1:p.Met47Val
NM_001320961.1:c.139A>G	NP_001307890.1:p.Met47Val
XM_017015708.1:c.139A>G	XP_016871197.1:p.Met47Val
XM_017015709.2:c.139A>G	XP_016871198.1:p.Met47Val
XM_017015710.1:c.139A>G	XP_016871199.1:p.Met47Val
XM_017015711.2:c.-3713A>G	XP_016871200.1:n.-3713A>G
XM_017015712.1:c.-3713A>G	XP_016871201.1:n.-3713A>G
XM_017015713.1:c.-3713A>G	XP_016871202.1:n.-3713A>G
XM_017015714.1:c.-3713A>G	XP_016871203.1:n.-3713A>G
XM_024447819.1:c.-3713A>G	XP_024303587.1:n.-3713A>G
NM_005204.4:c.139A>G MANE Select	NP_005195.2:p.Met47Val
NM_001320961.2:c.139A>G	NP_001307890.1:p.Met47Val