Canonical Allele Identifier: CA2148365868
Gene: TMED8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77339093G= , CM000676.2:g.77339093G= GRCh38
NC_000014.8:g.77805436G= , CM000676.1:g.77805436G= GRCh37
NC_000014.7:g.76875189G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216468.8:c.*2678C= MANE Select ENSP00000216468.7:n.*2678C=
ENST00000216468.7:c.*2678C= ENSP00000216468.7:n.*2678C=
XM_005267544.3:c.*2678C= XP_005267601.1:n.*2678C=
NM_001346131.1:c.*2678C= NP_001333060.1:n.*2678C=
NM_001346133.1:c.*2678C= NP_001333062.1:n.*2678C=
NM_001346134.1:c.*2678C= NP_001333063.1:n.*2678C=
NM_213601.2:c.*2678C= NP_998766.1:n.*2678C=
XM_017021224.1:c.*2678C= XP_016876713.1:n.*2678C=
NM_213601.3:c.*2678C= MANE Select NP_998766.1:n.*2678C=
NM_001346131.2:c.*2678C= NP_001333060.1:n.*2678C=
NM_001346133.2:c.*2678C= NP_001333062.1:n.*2678C=