Canonical Allele Identifier: CA487829388

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91739968C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273624C>G , CM000676.2:g.91273624C>G	GRCh38
NC_000014.8:g.91739968C>G , CM000676.1:g.91739968C>G	GRCh37
NC_000014.7:g.90809721C>G	NCBI36
NG_033118.1:g.149221G>C
NG_033118.2:g.149221G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5088G>C MANE Select	ENSP00000374507.6:p.Leu1696=
ENST00000331194.8:c.660G>C	ENSP00000330332.8:p.Leu220=
ENST00000334448.5:n.900G>C
ENST00000389857.10:c.5088G>C	ENSP00000374507.6:p.Leu1696=
ENST00000556726.5:c.1316G>C
NM_001080414.3:c.5088G>C	NP_001073883.2:p.Leu1696=
XM_011536796.1:c.4980G>C	XP_011535098.1:p.Leu1660=
XR_429316.2:n.5363G>C
XM_011536796.2:c.4980G>C	XP_011535098.1:p.Leu1660=
XM_017021336.1:c.2169G>C	XP_016876825.1:p.Leu723=
XR_429316.4:n.5361G>C
NM_001080414.4:c.5088G>C MANE Select	NP_001073883.2:p.Leu1696=