Canonical Allele Identifier: CA487829369

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91739935T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273591T>C , CM000676.2:g.91273591T>C	GRCh38
NC_000014.8:g.91739935T>C , CM000676.1:g.91739935T>C	GRCh37
NC_000014.7:g.90809688T>C	NCBI36
NG_033118.1:g.149254A>G
NG_033118.2:g.149254A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5121A>G MANE Select	ENSP00000374507.6:p.Pro1707=
ENST00000331194.8:c.693A>G	ENSP00000330332.8:p.Pro231=
ENST00000334448.5:n.933A>G
ENST00000389857.10:c.5121A>G	ENSP00000374507.6:p.Pro1707=
ENST00000556726.5:c.1349A>G
NM_001080414.3:c.5121A>G	NP_001073883.2:p.Pro1707=
XM_011536796.1:c.5013A>G	XP_011535098.1:p.Pro1671=
XR_429316.2:n.5396A>G
XM_011536796.2:c.5013A>G	XP_011535098.1:p.Pro1671=
XM_017021336.1:c.2202A>G	XP_016876825.1:p.Pro734=
XR_429316.4:n.5394A>G
NM_001080414.4:c.5121A>G MANE Select	NP_001073883.2:p.Pro1707=