Canonical Allele Identifier: CA2626125334

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91279316-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91279316A>G , CM000676.2:g.91279316A>G	GRCh38
NC_000014.8:g.91745660A>G , CM000676.1:g.91745660A>G	GRCh37
NC_000014.7:g.90815413A>G	NCBI36
NG_033118.1:g.143529T>C
NG_033118.2:g.143529T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.4700-10T>C MANE Select	ENSP00000374507.6:n.4700-10T>C
ENST00000331194.8:c.272-10T>C	ENSP00000330332.8:n.272-10T>C
ENST00000334448.5:n.512-10T>C
ENST00000389857.10:c.4700-10T>C	ENSP00000374507.6:n.4700-10T>C
ENST00000556726.5:c.928-10T>C
ENST00000557455.1:n.662T>C
NM_001080414.3:c.4700-10T>C	NP_001073883.2:n.4700-10T>C
XM_011536796.1:c.4592-10T>C	XP_011535098.1:n.4592-10T>C
XR_429316.2:n.4975-10T>C
XM_011536796.2:c.4592-10T>C	XP_011535098.1:n.4592-10T>C
XM_017021336.1:c.1781-10T>C	XP_016876825.1:n.1781-10T>C
XR_429316.4:n.4973-10T>C
NM_001080414.4:c.4700-10T>C MANE Select	NP_001073883.2:n.4700-10T>C