Canonical Allele Identifier: CA390613048

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91745626C>G (hg19) ; chr14:g.91279282C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91279282C>G , CM000676.2:g.91279282C>G	GRCh38
NC_000014.8:g.91745626C>G , CM000676.1:g.91745626C>G	GRCh37
NC_000014.7:g.90815379C>G	NCBI36
NG_033118.1:g.143563G>C
NG_033118.2:g.143563G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.4724G>C MANE Select	ENSP00000374507.6:p.Ser1575Thr
ENST00000331194.8:c.296G>C	ENSP00000330332.8:p.Ser99Thr
ENST00000334448.5:n.536G>C
ENST00000389857.10:c.4724G>C	ENSP00000374507.6:p.Ser1575Thr
ENST00000556726.5:c.952G>C
ENST00000557455.1:n.696G>C
NM_001080414.3:c.4724G>C	NP_001073883.2:p.Ser1575Thr
XM_011536796.1:c.4616G>C	XP_011535098.1:p.Ser1539Thr
XR_429316.2:n.4999G>C
XM_011536796.2:c.4616G>C	XP_011535098.1:p.Ser1539Thr
XM_017021336.1:c.1805G>C	XP_016876825.1:p.Ser602Thr
XR_429316.4:n.4997G>C
NM_001080414.4:c.4724G>C MANE Select	NP_001073883.2:p.Ser1575Thr