Canonical Allele Identifier: CA2154899671

Gene: CCDC88C

Linked Data

• dbSNP Id: rs1889772465

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272398G>C , CM000676.2:g.91272398G>C	GRCh38
NC_000014.8:g.91738742G>C , CM000676.1:g.91738742G>C	GRCh37
NC_000014.7:g.90808495G>C	NCBI36
NG_033118.1:g.150447C>G
NG_033118.2:g.150447C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*227C>G MANE Select	ENSP00000374507.6:n.*227C>G
ENST00000331194.8:c.*227C>G	ENSP00000330332.8:n.*227C>G
ENST00000389857.10:c.*227C>G	ENSP00000374507.6:n.*227C>G
ENST00000556726.5:c.2542C>G
NM_001080414.3:c.*227C>G	NP_001073883.2:n.*227C>G
XM_011536796.1:c.*227C>G	XP_011535098.1:n.*227C>G
XM_011536796.2:c.*227C>G	XP_011535098.1:n.*227C>G
XM_017021336.1:c.*227C>G	XP_016876825.1:n.*227C>G
NM_001080414.4:c.*227C>G MANE Select	NP_001073883.2:n.*227C>G