Canonical Allele Identifier: CA592448554

Gene: MAP3K8

Linked Data

• dbSNP Id: rs1223305025
• gnomAD v2: 10-30728158-T-TCTTAGGTCCC
• MyVariant Identifiers: chr10:g.30728158_30728159insCTTAGGTCCC (hg19) ; chr10:g.30439229_30439230insCTTAGGTCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30439229_30439230insCTTAGGTCCC , CM000672.2:g.30439229_30439230insCTTAGGTCCC	GRCh38
NC_000010.10:g.30728158_30728159insCTTAGGTCCC , CM000672.1:g.30728158_30728159insCTTAGGTCCC	GRCh37
NC_000010.9:g.30768164_30768165insCTTAGGTCCC	NCBI36
NG_029984.1:g.10209_10210insCTTAGGTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263056.6:c.291_292insCTTAGGTCCC MANE Select	ENSP00000263056.1:p.Phe98LeufsTer?
ENST00000263056.5:c.291_292insCTTAGGTCCC	ENSP00000263056.1:p.Phe98LeufsTer?
ENST00000375321.1:c.291_292insCTTAGGTCCC	ENSP00000364470.1:p.Phe98LeufsTer?
ENST00000375322.2:c.291_292insCTTAGGTCCC	ENSP00000364471.1:p.Phe98LeufsTer?
ENST00000413724.5:c.291_292insCTTAGGTCCC	ENSP00000391275.1:p.Phe98LeufsTer?
ENST00000415139.5:c.291_292insCTTAGGTCCC	ENSP00000409653.1:p.Phe98LeufsTer?
ENST00000430603.1:n.53_54insCTTAGGTCCC
ENST00000542547.5:c.291_292insCTTAGGTCCC	ENSP00000443610.1:p.Phe98LeufsTer?
NM_001244134.1:c.291_292insCTTAGGTCCC	NP_001231063.1:p.Phe98LeufsTer?
NM_005204.3:c.291_292insCTTAGGTCCC	NP_005195.2:p.Phe98LeufsTer?
XM_005252364.2:c.291_292insCTTAGGTCCC	XP_005252421.2:p.Phe98LeufsTer?
XM_011519308.1:c.606_607insCTTAGGTCCC	XP_011517610.1:p.Phe203LeufsTer?
XM_011519309.1:c.423+4481_423+4482insCTTAGGTCCC	XP_011517611.1:n.423+4481_423+4482insCTTAGGTCCC
XM_011519310.1:c.291_292insCTTAGGTCCC	XP_011517612.1:p.Phe98LeufsTer?
XM_011519311.1:c.291_292insCTTAGGTCCC	XP_011517613.1:p.Phe98LeufsTer?
XM_011519312.1:c.291_292insCTTAGGTCCC	XP_011517614.1:p.Phe98LeufsTer?
XM_011519313.1:c.291_292insCTTAGGTCCC	XP_011517615.1:p.Phe98LeufsTer?
XM_011519314.1:c.291_292insCTTAGGTCCC	XP_011517616.1:p.Phe98LeufsTer?
XM_011519315.1:c.291_292insCTTAGGTCCC	XP_011517617.1:p.Phe98LeufsTer?
NM_001320961.1:c.291_292insCTTAGGTCCC	NP_001307890.1:p.Phe98LeufsTer?
XM_017015708.1:c.291_292insCTTAGGTCCC	XP_016871197.1:p.Phe98LeufsTer?
XM_017015709.2:c.291_292insCTTAGGTCCC	XP_016871198.1:p.Phe98LeufsTer?
XM_017015710.1:c.291_292insCTTAGGTCCC	XP_016871199.1:p.Phe98LeufsTer?
XM_017015711.2:c.-3561_-3560insCTTAGGTCCC	XP_016871200.1:n.-3561_-3560insCTTAGGTCCC
XM_017015712.1:c.-3561_-3560insCTTAGGTCCC	XP_016871201.1:n.-3561_-3560insCTTAGGTCCC
XM_017015713.1:c.-3561_-3560insCTTAGGTCCC	XP_016871202.1:n.-3561_-3560insCTTAGGTCCC
XM_017015714.1:c.-3561_-3560insCTTAGGTCCC	XP_016871203.1:n.-3561_-3560insCTTAGGTCCC
XM_024447819.1:c.-3561_-3560insCTTAGGTCCC	XP_024303587.1:n.-3561_-3560insCTTAGGTCCC
NM_005204.4:c.291_292insCTTAGGTCCC MANE Select	NP_005195.2:p.Phe98LeufsTer?
NM_001320961.2:c.291_292insCTTAGGTCCC	NP_001307890.1:p.Phe98LeufsTer?