Canonical Allele Identifier: CA1139838758
Gene: CASZ1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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