Canonical Allele Identifier: CA2625741283
Gene: TMED10 HGNC NCBI

Linked Data

gnomAD v4: 14-75135059-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75135059G>T , CM000676.2:g.75135059G>T GRCh38
NC_000014.8:g.75601762G>T , CM000676.1:g.75601762G>T GRCh37
NC_000014.7:g.74671515G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000303575.9:c.539-53C>A MANE Select ENSP00000303145.4:n.539-53C>A
ENST00000303575.8:c.539-53C>A ENSP00000303145.4:n.539-53C>A
ENST00000555036.1:n.322-53C>A
ENST00000555873.1:c.*175-53C>A ENSP00000450726.1:n.*175-53C>A
ENST00000556969.5:n.246-53C>A
ENST00000557670.5:n.267-53C>A
NM_006827.5:c.539-53C>A NP_006818.3:n.539-53C>A
NM_006827.6:c.539-53C>A MANE Select NP_006818.3:n.539-53C>A
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