Canonical Allele Identifier: CA7277375
Gene: TMED10 HGNC NCBI

Linked Data

dbSNP Id: rs758722084
ExAC: 14:75601752 T / C
gnomAD v2: 14-75601752-T-C
gnomAD v4: 14-75135049-T-C
MyVariant Identifiers: chr14:g.75601752T>C (hg19) chr14:g.75135049T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75135049T>C , CM000676.2:g.75135049T>C GRCh38
NC_000014.8:g.75601752T>C , CM000676.1:g.75601752T>C GRCh37
NC_000014.7:g.74671505T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000303575.9:c.539-43A>G MANE Select ENSP00000303145.4:n.539-43A>G
ENST00000303575.8:c.539-43A>G ENSP00000303145.4:n.539-43A>G
ENST00000555036.1:n.322-43A>G
ENST00000555873.1:c.*175-43A>G ENSP00000450726.1:n.*175-43A>G
ENST00000556969.5:n.246-43A>G
ENST00000557670.5:n.267-43A>G
NM_006827.5:c.539-43A>G NP_006818.3:n.539-43A>G
NM_006827.6:c.539-43A>G MANE Select NP_006818.3:n.539-43A>G
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