Canonical Allele Identifier: CA390610837

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91273593-G-A
• MyVariant Identifiers: chr14:g.91739937G>A (hg19) ; chr14:g.91273593G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273593G>A , CM000676.2:g.91273593G>A	GRCh38
NC_000014.8:g.91739937G>A , CM000676.1:g.91739937G>A	GRCh37
NC_000014.7:g.90809690G>A	NCBI36
NG_033118.1:g.149252C>T
NG_033118.2:g.149252C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5119C>T MANE Select	ENSP00000374507.6:p.Pro1707Ser
ENST00000331194.8:c.691C>T	ENSP00000330332.8:p.Pro231Ser
ENST00000334448.5:n.931C>T
ENST00000389857.10:c.5119C>T	ENSP00000374507.6:p.Pro1707Ser
ENST00000556726.5:c.1347C>T
NM_001080414.3:c.5119C>T	NP_001073883.2:p.Pro1707Ser
XM_011536796.1:c.5011C>T	XP_011535098.1:p.Pro1671Ser
XR_429316.2:n.5394C>T
XM_011536796.2:c.5011C>T	XP_011535098.1:p.Pro1671Ser
XM_017021336.1:c.2200C>T	XP_016876825.1:p.Pro734Ser
XR_429316.4:n.5392C>T
NM_001080414.4:c.5119C>T MANE Select	NP_001073883.2:p.Pro1707Ser