Canonical Allele Identifier: CA390613018

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91279272-G-T
• MyVariant Identifiers: chr14:g.91745616G>T (hg19) ; chr14:g.91279272G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91279272G>T , CM000676.2:g.91279272G>T	GRCh38
NC_000014.8:g.91745616G>T , CM000676.1:g.91745616G>T	GRCh37
NC_000014.7:g.90815369G>T	NCBI36
NG_033118.1:g.143573C>A
NG_033118.2:g.143573C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.4734C>A MANE Select	ENSP00000374507.6:p.Asn1578Lys
ENST00000331194.8:c.306C>A	ENSP00000330332.8:p.Asn102Lys
ENST00000334448.5:n.546C>A
ENST00000389857.10:c.4734C>A	ENSP00000374507.6:p.Asn1578Lys
ENST00000556726.5:c.962C>A
ENST00000557455.1:n.706C>A
NM_001080414.3:c.4734C>A	NP_001073883.2:p.Asn1578Lys
XM_011536796.1:c.4626C>A	XP_011535098.1:p.Asn1542Lys
XR_429316.2:n.5009C>A
XM_011536796.2:c.4626C>A	XP_011535098.1:p.Asn1542Lys
XM_017021336.1:c.1815C>A	XP_016876825.1:p.Asn605Lys
XR_429316.4:n.5007C>A
NM_001080414.4:c.4734C>A MANE Select	NP_001073883.2:p.Asn1578Lys