Canonical Allele Identifier: CA1153368313
Gene: CASZ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10736809T>G , CM000663.2:g.10736809T>G GRCh38
NC_000001.10:g.10796866T>G , CM000663.1:g.10796866T>G GRCh37
NC_000001.9:g.10719453T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377022.8:c.-77+23892A>C MANE Select ENSP00000366221.3:n.-77+23892A>C
ENST00000344008.5:c.-77+23892A>C ENSP00000339445.5:n.-77+23892A>C
ENST00000377022.7:c.-77+23892A>C ENSP00000366221.3:n.-77+23892A>C
NM_001079843.2:c.-77+23892A>C NP_001073312.1:n.-77+23892A>C
NM_017766.4:c.-77+23892A>C NP_060236.3:n.-77+23892A>C
XM_006710712.2:c.-77+23892A>C XP_006710775.1:n.-77+23892A>C
XM_017001540.2:c.-77+23892A>C XP_016857029.1:n.-77+23892A>C
XM_017001541.2:c.-77+23892A>C XP_016857030.1:n.-77+23892A>C
NM_001079843.3:c.-77+23892A>C MANE Select NP_001073312.1:n.-77+23892A>C
NM_017766.5:c.-77+23892A>C NP_060236.3:n.-77+23892A>C