Canonical Allele Identifier: CA390610699

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91739872A>C (hg19) ; chr14:g.91273528A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273528A>C , CM000676.2:g.91273528A>C	GRCh38
NC_000014.8:g.91739872A>C , CM000676.1:g.91739872A>C	GRCh37
NC_000014.7:g.90809625A>C	NCBI36
NG_033118.1:g.149317T>G
NG_033118.2:g.149317T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.5184T>G MANE Select	ENSP00000374507.6:p.Phe1728Leu
ENST00000331194.8:c.756T>G	ENSP00000330332.8:p.Phe252Leu
ENST00000334448.5:n.996T>G
ENST00000389857.10:c.5184T>G	ENSP00000374507.6:p.Phe1728Leu
ENST00000556726.5:c.1412T>G
NM_001080414.3:c.5184T>G	NP_001073883.2:p.Phe1728Leu
XM_011536796.1:c.5076T>G	XP_011535098.1:p.Phe1692Leu
XR_429316.2:n.5459T>G
XM_011536796.2:c.5076T>G	XP_011535098.1:p.Phe1692Leu
XM_017021336.1:c.2265T>G	XP_016876825.1:p.Phe755Leu
XR_429316.4:n.5457T>G
NM_001080414.4:c.5184T>G MANE Select	NP_001073883.2:p.Phe1728Leu