Canonical Allele Identifier: CA13965422

Gene: TMEM63C

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77218327C>G , CM000676.2:g.77218327C>G	GRCh38
NC_000014.8:g.77684670C>G , CM000676.1:g.77684670C>G	GRCh37
NC_000014.7:g.76754423C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298351.5:c.-13-474C>G MANE Select	ENSP00000298351.4:n.-13-474C>G
ENST00000298351.4:c.-13-474C>G	ENSP00000298351.4:n.-13-474C>G
ENST00000554346.5:c.-13-474C>G	ENSP00000451237.1:n.-13-474C>G
ENST00000554766.5:c.-13-474C>G	ENSP00000451842.1:n.-13-474C>G
ENST00000555338.5:c.-13-474C>G	ENSP00000451398.1:n.-13-474C>G
ENST00000556514.5:c.-13-474C>G	ENSP00000451404.1:n.-13-474C>G
ENST00000557408.5:c.-13-474C>G	ENSP00000450879.1:n.-13-474C>G
ENST00000557752.1:c.137-474C>G	ENSP00000456507.1:n.137-474C>G
NM_020431.3:c.-13-474C>G	NP_065164.2:n.-13-474C>G
NM_020431.4:c.-13-474C>G MANE Select	NP_065164.2:n.-13-474C>G