Canonical Allele Identifier: CA390610307

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91273434-C-A
• MyVariant Identifiers: chr14:g.91739778C>A (hg19) ; chr14:g.91273434C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273434C>A , CM000676.2:g.91273434C>A	GRCh38
NC_000014.8:g.91739778C>A , CM000676.1:g.91739778C>A	GRCh37
NC_000014.7:g.90809531C>A	NCBI36
NG_033118.1:g.149411G>T
NG_033118.2:g.149411G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.5278G>T MANE Select	ENSP00000374507.6:p.Ala1760Ser
ENST00000331194.8:c.850G>T	ENSP00000330332.8:p.Ala284Ser
ENST00000389857.10:c.5278G>T	ENSP00000374507.6:p.Ala1760Ser
ENST00000556726.5:c.1506G>T
NM_001080414.3:c.5278G>T	NP_001073883.2:p.Ala1760Ser
XM_011536796.1:c.5170G>T	XP_011535098.1:p.Ala1724Ser
XM_011536796.2:c.5170G>T	XP_011535098.1:p.Ala1724Ser
XM_017021336.1:c.2359G>T	XP_016876825.1:p.Ala787Ser
NM_001080414.4:c.5278G>T MANE Select	NP_001073883.2:p.Ala1760Ser