Canonical Allele Identifier: CA2154899738
Gene: CCDC88C HGNC NCBI

Linked Data

dbSNP Id: rs1889774599
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272455T>G , CM000676.2:g.91272455T>G GRCh38
NC_000014.8:g.91738799T>G , CM000676.1:g.91738799T>G GRCh37
NC_000014.7:g.90808552T>G NCBI36
NG_033118.1:g.150390A>C
NG_033118.2:g.150390A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.*170A>C MANE Select ENSP00000374507.6:n.*170A>C
ENST00000331194.8:c.*170A>C ENSP00000330332.8:n.*170A>C
ENST00000389857.10:c.*170A>C ENSP00000374507.6:n.*170A>C
ENST00000556726.5:c.2485A>C
NM_001080414.3:c.*170A>C NP_001073883.2:n.*170A>C
XM_011536796.1:c.*170A>C XP_011535098.1:n.*170A>C
XM_011536796.2:c.*170A>C XP_011535098.1:n.*170A>C
XM_017021336.1:c.*170A>C XP_016876825.1:n.*170A>C
NM_001080414.4:c.*170A>C MANE Select NP_001073883.2:n.*170A>C
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