Canonical Allele Identifier: CA390623698

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91772261G>C (hg19) ; chr14:g.91305917G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91305917G>C , CM000676.2:g.91305917G>C	GRCh38
NC_000014.8:g.91772261G>C , CM000676.1:g.91772261G>C	GRCh37
NC_000014.7:g.90842014G>C	NCBI36
NG_033118.1:g.116928C>G
NG_033118.2:g.116928C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3205C>G MANE Select	ENSP00000374507.6:p.Leu1069Val
ENST00000389857.10:c.3205C>G	ENSP00000374507.6:p.Leu1069Val
NM_001080414.3:c.3205C>G	NP_001073883.2:p.Leu1069Val
XM_005267691.3:c.3205C>G	XP_005267748.1:p.Leu1069Val
XM_011536796.1:c.3097C>G	XP_011535098.1:p.Leu1033Val
XR_429316.2:n.3333C>G
XR_943459.1:n.3333C>G
XM_005267691.5:c.3205C>G	XP_005267748.1:p.Leu1069Val
XM_011536796.2:c.3097C>G	XP_011535098.1:p.Leu1033Val
XM_017021335.2:c.3205C>G	XP_016876824.1:p.Leu1069Val
XM_017021336.1:c.286C>G	XP_016876825.1:p.Leu96Val
XR_429316.4:n.3331C>G
NM_001080414.4:c.3205C>G MANE Select	NP_001073883.2:p.Leu1069Val