Canonical Allele Identifier: CA487829242

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91273426-G-T
• MyVariant Identifiers: chr14:g.91739770G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273426G>T , CM000676.2:g.91273426G>T	GRCh38
NC_000014.8:g.91739770G>T , CM000676.1:g.91739770G>T	GRCh37
NC_000014.7:g.90809523G>T	NCBI36
NG_033118.1:g.149419C>A
NG_033118.2:g.149419C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5286C>A MANE Select	ENSP00000374507.6:p.Ala1762=
ENST00000331194.8:c.858C>A	ENSP00000330332.8:p.Ala286=
ENST00000389857.10:c.5286C>A	ENSP00000374507.6:p.Ala1762=
ENST00000556726.5:c.1514C>A
NM_001080414.3:c.5286C>A	NP_001073883.2:p.Ala1762=
XM_011536796.1:c.5178C>A	XP_011535098.1:p.Ala1726=
XM_011536796.2:c.5178C>A	XP_011535098.1:p.Ala1726=
XM_017021336.1:c.2367C>A	XP_016876825.1:p.Ala789=
NM_001080414.4:c.5286C>A MANE Select	NP_001073883.2:p.Ala1762=