Canonical Allele Identifier: CA390610749

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91273551-C-A
• MyVariant Identifiers: chr14:g.91739895C>A (hg19) ; chr14:g.91273551C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273551C>A , CM000676.2:g.91273551C>A	GRCh38
NC_000014.8:g.91739895C>A , CM000676.1:g.91739895C>A	GRCh37
NC_000014.7:g.90809648C>A	NCBI36
NG_033118.1:g.149294G>T
NG_033118.2:g.149294G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5161G>T MANE Select	ENSP00000374507.6:p.Gly1721Trp
ENST00000331194.8:c.733G>T	ENSP00000330332.8:p.Gly245Trp
ENST00000334448.5:n.973G>T
ENST00000389857.10:c.5161G>T	ENSP00000374507.6:p.Gly1721Trp
ENST00000556726.5:c.1389G>T
NM_001080414.3:c.5161G>T	NP_001073883.2:p.Gly1721Trp
XM_011536796.1:c.5053G>T	XP_011535098.1:p.Gly1685Trp
XR_429316.2:n.5436G>T
XM_011536796.2:c.5053G>T	XP_011535098.1:p.Gly1685Trp
XM_017021336.1:c.2242G>T	XP_016876825.1:p.Gly748Trp
XR_429316.4:n.5434G>T
NM_001080414.4:c.5161G>T MANE Select	NP_001073883.2:p.Gly1721Trp