Canonical Allele Identifier: CA2626125204

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91279215-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91279215G>C , CM000676.2:g.91279215G>C	GRCh38
NC_000014.8:g.91745559G>C , CM000676.1:g.91745559G>C	GRCh37
NC_000014.7:g.90815312G>C	NCBI36
NG_033118.1:g.143630C>G
NG_033118.2:g.143630C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.4768+23C>G MANE Select	ENSP00000374507.6:n.4768+23C>G
ENST00000331194.8:c.340+23C>G	ENSP00000330332.8:n.340+23C>G
ENST00000334448.5:n.580+23C>G
ENST00000389857.10:c.4768+23C>G	ENSP00000374507.6:n.4768+23C>G
ENST00000556726.5:c.996+23C>G
ENST00000557455.1:n.740+23C>G
NM_001080414.3:c.4768+23C>G	NP_001073883.2:n.4768+23C>G
XM_011536796.1:c.4660+23C>G	XP_011535098.1:n.4660+23C>G
XR_429316.2:n.5043+23C>G
XM_011536796.2:c.4660+23C>G	XP_011535098.1:n.4660+23C>G
XM_017021336.1:c.1849+23C>G	XP_016876825.1:n.1849+23C>G
XR_429316.4:n.5041+23C>G
NM_001080414.4:c.4768+23C>G MANE Select	NP_001073883.2:n.4768+23C>G