Canonical Allele Identifier: CA390613288

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91747839G>C (hg19) ; chr14:g.91281495G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91281495G>C , CM000676.2:g.91281495G>C	GRCh38
NC_000014.8:g.91747839G>C , CM000676.1:g.91747839G>C	GRCh37
NC_000014.7:g.90817592G>C	NCBI36
NG_033118.1:g.141350C>G
NG_033118.2:g.141350C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.4661C>G MANE Select	ENSP00000374507.6:p.Pro1554Arg
ENST00000331194.8:c.233C>G	ENSP00000330332.8:p.Pro78Arg
ENST00000334448.5:n.326C>G
ENST00000389857.10:c.4661C>G	ENSP00000374507.6:p.Pro1554Arg
ENST00000556726.5:c.889C>G
NM_001080414.3:c.4661C>G	NP_001073883.2:p.Pro1554Arg
XM_011536796.1:c.4553C>G	XP_011535098.1:p.Pro1518Arg
XR_429316.2:n.4789C>G
XR_943459.1:n.4789C>G
XM_011536796.2:c.4553C>G	XP_011535098.1:p.Pro1518Arg
XM_017021335.2:c.4661C>G	XP_016876824.1:p.Pro1554Arg
XM_017021336.1:c.1742C>G	XP_016876825.1:p.Pro581Arg
XR_429316.4:n.4787C>G
NM_001080414.4:c.4661C>G MANE Select	NP_001073883.2:p.Pro1554Arg