Canonical Allele Identifier: CA2695239926
Gene: CASP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15524572_15524590del , CM000663.2:g.15524572_15524590del GRCh38
NC_000001.10:g.15851067_15851085del , CM000663.1:g.15851067_15851085del GRCh37
NC_000001.9:g.15723654_15723672del NCBI36
NG_029188.1:g.5203_5221del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375890.8:c.-123_-118+13del
ENST00000447522.5:c.-118+264_-118+282del ENSP00000396540.1:n.-118+264_-118+282del
ENST00000469637.1:c.-239+1603_-239+1621del ENSP00000480785.1:n.-239+1603_-239+1621del
NM_032996.3:c.-123_-118+13del
XM_005246014.2:c.-118+264_-118+282del XP_005246071.1:n.-118+264_-118+282del
XM_011542272.1:c.-118+1603_-118+1621del XP_011540574.1:n.-118+1603_-118+1621del