Canonical Allele Identifier: CA390623131

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91772137G>C (hg19) ; chr14:g.91305793G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91305793G>C , CM000676.2:g.91305793G>C	GRCh38
NC_000014.8:g.91772137G>C , CM000676.1:g.91772137G>C	GRCh37
NC_000014.7:g.90841890G>C	NCBI36
NG_033118.1:g.117052C>G
NG_033118.2:g.117052C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3329C>G MANE Select	ENSP00000374507.6:p.Thr1110Arg
ENST00000389857.10:c.3329C>G	ENSP00000374507.6:p.Thr1110Arg
NM_001080414.3:c.3329C>G	NP_001073883.2:p.Thr1110Arg
XM_005267691.3:c.3329C>G	XP_005267748.1:p.Thr1110Arg
XM_011536796.1:c.3221C>G	XP_011535098.1:p.Thr1074Arg
XR_429316.2:n.3457C>G
XR_943459.1:n.3457C>G
XM_005267691.5:c.3329C>G	XP_005267748.1:p.Thr1110Arg
XM_011536796.2:c.3221C>G	XP_011535098.1:p.Thr1074Arg
XM_017021335.2:c.3329C>G	XP_016876824.1:p.Thr1110Arg
XM_017021336.1:c.410C>G	XP_016876825.1:p.Thr137Arg
XR_429316.4:n.3455C>G
NM_001080414.4:c.3329C>G MANE Select	NP_001073883.2:p.Thr1110Arg