Canonical Allele Identifier: CA7310042

Gene: CCDC88C

Linked Data

• dbSNP Id: rs776504122
• ExAC: 14:91804444 G / A
• gnomAD v2: 14-91804444-G-A
• gnomAD v3: 14-91338100-G-A
• gnomAD v4: 14-91338100-G-A
• MyVariant Identifiers: chr14:g.91804444G>A (hg19) ; chr14:g.91338100G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91338100G>A , CM000676.2:g.91338100G>A	GRCh38
NC_000014.8:g.91804444G>A , CM000676.1:g.91804444G>A	GRCh37
NC_000014.7:g.90874197G>A	NCBI36
NG_033118.1:g.84745C>T
NG_033118.2:g.84745C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.955C>T MANE Select	ENSP00000374507.6:p.Arg319Trp
ENST00000389857.10:c.955C>T	ENSP00000374507.6:p.Arg319Trp
ENST00000554051.1:n.432C>T
NM_001080414.3:c.955C>T	NP_001073883.2:p.Arg319Trp
XM_005267691.3:c.955C>T	XP_005267748.1:p.Arg319Trp
XM_011536796.1:c.847C>T	XP_011535098.1:p.Arg283Trp
XR_429316.2:n.1083C>T
XR_943459.1:n.1083C>T
XM_005267691.5:c.955C>T	XP_005267748.1:p.Arg319Trp
XM_011536796.2:c.847C>T	XP_011535098.1:p.Arg283Trp
XM_017021335.2:c.955C>T	XP_016876824.1:p.Arg319Trp
XM_017021337.2:c.955C>T	XP_016876826.1:p.Arg319Trp
XR_429316.4:n.1081C>T
NM_001080414.4:c.955C>T MANE Select	NP_001073883.2:p.Arg319Trp