Canonical Allele Identifier: CA390608589
Gene: CCDC88C HGNC NCBI

Linked Data

dbSNP Id: rs1166017807

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272824G>A , CM000676.2:g.91272824G>A GRCh38
NC_000014.8:g.91739168G>A , CM000676.1:g.91739168G>A GRCh37
NC_000014.7:g.90808921G>A NCBI36
NG_033118.1:g.150021C>T
NG_033118.2:g.150021C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.5888C>T MANE Select ENSP00000374507.6:p.Ser1963Leu
ENST00000331194.8:c.1322C>T ENSP00000330332.8:p.Ser441Leu
ENST00000389857.10:c.5888C>T ENSP00000374507.6:p.Ser1963Leu
ENST00000556726.5:c.2116C>T
NM_001080414.3:c.5888C>T NP_001073883.2:p.Ser1963Leu
XM_011536796.1:c.5780C>T XP_011535098.1:p.Ser1927Leu
XM_011536796.2:c.5780C>T XP_011535098.1:p.Ser1927Leu
XM_017021336.1:c.2969C>T XP_016876825.1:p.Ser990Leu
NM_001080414.4:c.5888C>T MANE Select NP_001073883.2:p.Ser1963Leu