Canonical Allele Identifier: CA2148365857

Gene: TMED8

Linked Data

• dbSNP Id: rs1892831488

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77339050T>C , CM000676.2:g.77339050T>C	GRCh38
NC_000014.8:g.77805393T>C , CM000676.1:g.77805393T>C	GRCh37
NC_000014.7:g.76875146T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216468.8:c.*2721A>G MANE Select	ENSP00000216468.7:n.*2721A>G
ENST00000216468.7:c.*2721A>G	ENSP00000216468.7:n.*2721A>G
XM_005267544.3:c.*2721A>G	XP_005267601.1:n.*2721A>G
NM_001346131.1:c.*2721A>G	NP_001333060.1:n.*2721A>G
NM_001346133.1:c.*2721A>G	NP_001333062.1:n.*2721A>G
NM_001346134.1:c.*2721A>G	NP_001333063.1:n.*2721A>G
NM_213601.2:c.*2721A>G	NP_998766.1:n.*2721A>G
XM_017021224.1:c.*2721A>G	XP_016876713.1:n.*2721A>G
NM_213601.3:c.*2721A>G MANE Select	NP_998766.1:n.*2721A>G
NM_001346131.2:c.*2721A>G	NP_001333060.1:n.*2721A>G
NM_001346133.2:c.*2721A>G	NP_001333062.1:n.*2721A>G