Canonical Allele Identifier: CA390612039

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91744346G>C (hg19) ; chr14:g.91278002G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91278002G>C , CM000676.2:g.91278002G>C	GRCh38
NC_000014.8:g.91744346G>C , CM000676.1:g.91744346G>C	GRCh37
NC_000014.7:g.90814099G>C	NCBI36
NG_033118.1:g.144843C>G
NG_033118.2:g.144843C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.4978C>G MANE Select	ENSP00000374507.6:p.Pro1660Ala
ENST00000331194.8:c.550C>G	ENSP00000330332.8:p.Pro184Ala
ENST00000334448.5:n.790C>G
ENST00000389857.10:c.4978C>G	ENSP00000374507.6:p.Pro1660Ala
ENST00000556726.5:c.1206C>G
NM_001080414.3:c.4978C>G	NP_001073883.2:p.Pro1660Ala
XM_011536796.1:c.4870C>G	XP_011535098.1:p.Pro1624Ala
XR_429316.2:n.5253C>G
XM_011536796.2:c.4870C>G	XP_011535098.1:p.Pro1624Ala
XM_017021336.1:c.2059C>G	XP_016876825.1:p.Pro687Ala
XR_429316.4:n.5251C>G
NM_001080414.4:c.4978C>G MANE Select	NP_001073883.2:p.Pro1660Ala