Canonical Allele Identifier: CA708731942

Gene: TMED8

Linked Data

• dbSNP Id: rs1426058295
• MyVariant Identifiers: chr14:g.77805370G>C (hg19) ; chr14:g.77339027G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77339027G>C , CM000676.2:g.77339027G>C	GRCh38
NC_000014.8:g.77805370G>C , CM000676.1:g.77805370G>C	GRCh37
NC_000014.7:g.76875123G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216468.8:c.*2744C>G MANE Select	ENSP00000216468.7:n.*2744C>G
ENST00000216468.7:c.*2744C>G	ENSP00000216468.7:n.*2744C>G
XM_005267544.3:c.*2744C>G	XP_005267601.1:n.*2744C>G
NM_001346131.1:c.*2744C>G	NP_001333060.1:n.*2744C>G
NM_001346133.1:c.*2744C>G	NP_001333062.1:n.*2744C>G
NM_001346134.1:c.*2744C>G	NP_001333063.1:n.*2744C>G
NM_213601.2:c.*2744C>G	NP_998766.1:n.*2744C>G
XM_017021224.1:c.*2744C>G	XP_016876713.1:n.*2744C>G
NM_213601.3:c.*2744C>G MANE Select	NP_998766.1:n.*2744C>G
NM_001346131.2:c.*2744C>G	NP_001333060.1:n.*2744C>G
NM_001346133.2:c.*2744C>G	NP_001333062.1:n.*2744C>G