Canonical Allele Identifier: CA390631151

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91779983A>T (hg19) ; chr14:g.91313639A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91313639A>T , CM000676.2:g.91313639A>T	GRCh38
NC_000014.8:g.91779983A>T , CM000676.1:g.91779983A>T	GRCh37
NC_000014.7:g.90849736A>T	NCBI36
NG_033118.1:g.109206T>A
NG_033118.2:g.109206T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.2177T>A MANE Select	ENSP00000374507.6:p.Met726Lys
ENST00000389857.10:c.2177T>A	ENSP00000374507.6:p.Met726Lys
NM_001080414.3:c.2177T>A	NP_001073883.2:p.Met726Lys
XM_005267691.3:c.2177T>A	XP_005267748.1:p.Met726Lys
XM_011536796.1:c.2069T>A	XP_011535098.1:p.Met690Lys
XR_429316.2:n.2305T>A
XR_943459.1:n.2305T>A
XM_005267691.5:c.2177T>A	XP_005267748.1:p.Met726Lys
XM_011536796.2:c.2069T>A	XP_011535098.1:p.Met690Lys
XM_017021335.2:c.2177T>A	XP_016876824.1:p.Met726Lys
XM_017021337.2:c.2177T>A	XP_016876826.1:p.Met726Lys
XR_429316.4:n.2303T>A
NM_001080414.4:c.2177T>A MANE Select	NP_001073883.2:p.Met726Lys