Canonical Allele Identifier: CA263805288

Gene: TMED8

Linked Data

• dbSNP Id: rs528569685
• gnomAD v3: 14-77338976-A-G
• gnomAD v4: 14-77338976-A-G
• MyVariant Identifiers: chr14:g.77805319A>G (hg19) ; chr14:g.77338976A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77338976A>G , CM000676.2:g.77338976A>G	GRCh38
NC_000014.8:g.77805319A>G , CM000676.1:g.77805319A>G	GRCh37
NC_000014.7:g.76875072A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216468.8:c.*2795T>C MANE Select	ENSP00000216468.7:n.*2795T>C
ENST00000216468.7:c.*2795T>C	ENSP00000216468.7:n.*2795T>C
XM_005267544.3:c.*2795T>C	XP_005267601.1:n.*2795T>C
NM_001346131.1:c.*2795T>C	NP_001333060.1:n.*2795T>C
NM_001346133.1:c.*2795T>C	NP_001333062.1:n.*2795T>C
NM_001346134.1:c.*2795T>C	NP_001333063.1:n.*2795T>C
NM_213601.2:c.*2795T>C	NP_998766.1:n.*2795T>C
XM_017021224.1:c.*2795T>C	XP_016876713.1:n.*2795T>C
NM_213601.3:c.*2795T>C MANE Select	NP_998766.1:n.*2795T>C
NM_001346131.2:c.*2795T>C	NP_001333060.1:n.*2795T>C
NM_001346133.2:c.*2795T>C	NP_001333062.1:n.*2795T>C