Canonical Allele Identifier: CA2148365880

Gene: TMED8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77339142C= , CM000676.2:g.77339142C=	GRCh38
NC_000014.8:g.77805485C= , CM000676.1:g.77805485C=	GRCh37
NC_000014.7:g.76875238C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216468.8:c.*2629G= MANE Select	ENSP00000216468.7:n.*2629G=
ENST00000216468.7:c.*2629G=	ENSP00000216468.7:n.*2629G=
XM_005267544.3:c.*2629G=	XP_005267601.1:n.*2629G=
NM_001346131.1:c.*2629G=	NP_001333060.1:n.*2629G=
NM_001346133.1:c.*2629G=	NP_001333062.1:n.*2629G=
NM_001346134.1:c.*2629G=	NP_001333063.1:n.*2629G=
NM_213601.2:c.*2629G=	NP_998766.1:n.*2629G=
XM_017021224.1:c.*2629G=	XP_016876713.1:n.*2629G=
NM_213601.3:c.*2629G= MANE Select	NP_998766.1:n.*2629G=
NM_001346131.2:c.*2629G=	NP_001333060.1:n.*2629G=
NM_001346133.2:c.*2629G=	NP_001333062.1:n.*2629G=