Canonical Allele Identifier: CA7309391

Gene: CCDC88C

Linked Data

• ClinVar Variation Id: 2836152
• ClinVar RCV Id: RCV003689935
• dbSNP Id: rs17127220
• ExAC: 14:91772121 G / C
• gnomAD v2: 14-91772121-G-C
• gnomAD v3: 14-91305777-G-C
• gnomAD v4: 14-91305777-G-C
• MyVariant Identifiers: chr14:g.91772121G>C (hg19) ; chr14:g.91305777G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91305777G>C , CM000676.2:g.91305777G>C	GRCh38
NC_000014.8:g.91772121G>C , CM000676.1:g.91772121G>C	GRCh37
NC_000014.7:g.90841874G>C	NCBI36
NG_033118.1:g.117068C>G
NG_033118.2:g.117068C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3345C>G MANE Select	ENSP00000374507.6:p.Thr1115=
ENST00000389857.10:c.3345C>G	ENSP00000374507.6:p.Thr1115=
NM_001080414.3:c.3345C>G	NP_001073883.2:p.Thr1115=
XM_005267691.3:c.3345C>G	XP_005267748.1:p.Thr1115=
XM_011536796.1:c.3237C>G	XP_011535098.1:p.Thr1079=
XR_429316.2:n.3473C>G
XR_943459.1:n.3473C>G
XM_005267691.5:c.3345C>G	XP_005267748.1:p.Thr1115=
XM_011536796.2:c.3237C>G	XP_011535098.1:p.Thr1079=
XM_017021335.2:c.3345C>G	XP_016876824.1:p.Thr1115=
XM_017021336.1:c.426C>G	XP_016876825.1:p.Thr142=
XR_429316.4:n.3471C>G
NM_001080414.4:c.3345C>G MANE Select	NP_001073883.2:p.Thr1115=