Canonical Allele Identifier: CA2148365828
Gene: TMED8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77338956A= , CM000676.2:g.77338956A= GRCh38
NC_000014.8:g.77805299A= , CM000676.1:g.77805299A= GRCh37
NC_000014.7:g.76875052A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216468.8:c.*2815T= MANE Select ENSP00000216468.7:n.*2815T=
ENST00000216468.7:c.*2815T= ENSP00000216468.7:n.*2815T=
XM_005267544.3:c.*2815T= XP_005267601.1:n.*2815T=
NM_001346131.1:c.*2815T= NP_001333060.1:n.*2815T=
NM_001346133.1:c.*2815T= NP_001333062.1:n.*2815T=
NM_001346134.1:c.*2815T= NP_001333063.1:n.*2815T=
NM_213601.2:c.*2815T= NP_998766.1:n.*2815T=
XM_017021224.1:c.*2815T= XP_016876713.1:n.*2815T=
NM_213601.3:c.*2815T= MANE Select NP_998766.1:n.*2815T=
NM_001346131.2:c.*2815T= NP_001333060.1:n.*2815T=
NM_001346133.2:c.*2815T= NP_001333062.1:n.*2815T=