Canonical Allele Identifier: CA2148365824

Gene: TMED8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77338945_77338949delinsATCTC , CM000676.2:g.77338945_77338949delinsATCTC	GRCh38
NC_000014.8:g.77805288_77805292delinsATCTC , CM000676.1:g.77805288_77805292delinsATCTC	GRCh37
NC_000014.7:g.76875041_76875045delinsATCTC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216468.8:c.*2822_*2826delinsGAGAT MANE Select	ENSP00000216468.7:n.*2822_*2826delinsGAGAT
ENST00000216468.7:c.*2822_*2826delinsGAGAT	ENSP00000216468.7:n.*2822_*2826delinsGAGAT
XM_005267544.3:c.*2822_*2826delinsGAGAT	XP_005267601.1:n.*2822_*2826delinsGAGAT
NM_001346131.1:c.*2822_*2826delinsGAGAT	NP_001333060.1:n.*2822_*2826delinsGAGAT
NM_001346133.1:c.*2822_*2826delinsGAGAT	NP_001333062.1:n.*2822_*2826delinsGAGAT
NM_001346134.1:c.*2822_*2826delinsGAGAT	NP_001333063.1:n.*2822_*2826delinsGAGAT
NM_213601.2:c.*2822_*2826delinsGAGAT	NP_998766.1:n.*2822_*2826delinsGAGAT
XM_017021224.1:c.*2822_*2826delinsGAGAT	XP_016876713.1:n.*2822_*2826delinsGAGAT
NM_213601.3:c.*2822_*2826delinsGAGAT MANE Select	NP_998766.1:n.*2822_*2826delinsGAGAT
NM_001346131.2:c.*2822_*2826delinsGAGAT	NP_001333060.1:n.*2822_*2826delinsGAGAT
NM_001346133.2:c.*2822_*2826delinsGAGAT	NP_001333062.1:n.*2822_*2826delinsGAGAT