Canonical Allele Identifier: CA2148365844

Gene: TMED8

Linked Data

• dbSNP Id: rs1892828362

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77338997T>G , CM000676.2:g.77338997T>G	GRCh38
NC_000014.8:g.77805340T>G , CM000676.1:g.77805340T>G	GRCh37
NC_000014.7:g.76875093T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216468.8:c.*2774A>C MANE Select	ENSP00000216468.7:n.*2774A>C
ENST00000216468.7:c.*2774A>C	ENSP00000216468.7:n.*2774A>C
XM_005267544.3:c.*2774A>C	XP_005267601.1:n.*2774A>C
NM_001346131.1:c.*2774A>C	NP_001333060.1:n.*2774A>C
NM_001346133.1:c.*2774A>C	NP_001333062.1:n.*2774A>C
NM_001346134.1:c.*2774A>C	NP_001333063.1:n.*2774A>C
NM_213601.2:c.*2774A>C	NP_998766.1:n.*2774A>C
XM_017021224.1:c.*2774A>C	XP_016876713.1:n.*2774A>C
NM_213601.3:c.*2774A>C MANE Select	NP_998766.1:n.*2774A>C
NM_001346131.2:c.*2774A>C	NP_001333060.1:n.*2774A>C
NM_001346133.2:c.*2774A>C	NP_001333062.1:n.*2774A>C