Canonical Allele Identifier: CA390611979

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91804502G>C (hg19) ; chr14:g.91338158G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91338158G>C , CM000676.2:g.91338158G>C	GRCh38
NC_000014.8:g.91804502G>C , CM000676.1:g.91804502G>C	GRCh37
NC_000014.7:g.90874255G>C	NCBI36
NG_033118.1:g.84687C>G
NG_033118.2:g.84687C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.897C>G MANE Select	ENSP00000374507.6:p.Ile299Met
ENST00000389857.10:c.897C>G	ENSP00000374507.6:p.Ile299Met
ENST00000554051.1:n.374C>G
NM_001080414.3:c.897C>G	NP_001073883.2:p.Ile299Met
XM_005267691.3:c.897C>G	XP_005267748.1:p.Ile299Met
XM_011536796.1:c.789C>G	XP_011535098.1:p.Ile263Met
XR_429316.2:n.1025C>G
XR_943459.1:n.1025C>G
XM_005267691.5:c.897C>G	XP_005267748.1:p.Ile299Met
XM_011536796.2:c.789C>G	XP_011535098.1:p.Ile263Met
XM_017021335.2:c.897C>G	XP_016876824.1:p.Ile299Met
XM_017021337.2:c.897C>G	XP_016876826.1:p.Ile299Met
XR_429316.4:n.1023C>G
NM_001080414.4:c.897C>G MANE Select	NP_001073883.2:p.Ile299Met