Canonical Allele Identifier: CA2674273788
Gene: CERT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.75426473_75426480del , CM000667.2:g.75426473_75426480del GRCh38
NC_000005.9:g.74722298_74722305del , CM000667.1:g.74722298_74722305del GRCh37
NC_000005.8:g.74758054_74758061del NCBI36
NG_029492.1:g.90502_90509del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647512.2:n.779-2_784del
ENST00000261415.12:c.349-2_354del
ENST00000380494.10:c.141-2_146del
ENST00000405807.10:c.733-2_738del
ENST00000642225.1:c.349-2_354del
ENST00000642556.1:c.349-2_354del
ENST00000642809.1:c.349-2_354del
ENST00000643158.1:c.349-2_354del
ENST00000643773.1:c.-48-2_-43del
ENST00000643780.2:c.349-2_354del
ENST00000644072.2:c.349-2_354del
ENST00000644377.1:c.349-2_354del
ENST00000644445.1:c.349-2_354del
ENST00000644516.1:c.349-2_354del
ENST00000644912.1:c.349-2_354del
ENST00000645483.1:c.349-2_354del
ENST00000645866.1:c.349-2_354del
ENST00000646302.1:c.349-2_354del
ENST00000646511.1:c.349-2_354del
ENST00000646713.1:c.349-2_354del
ENST00000647512.1:n.562-2_567del
ENST00000261415.11:c.349-2_354del
ENST00000380494.9:c.733-2_738del
ENST00000405807.8:c.349-2_354del
NM_001130105.1:c.733-2_738del
NM_005713.2:c.349-2_354del
NM_031361.2:c.349-2_354del
XM_006714513.1:c.349-2_354del
XM_011543090.1:c.349-2_354del
XM_011543091.1:c.349-2_354del
XM_006714513.3:c.349-2_354del
XM_011543090.3:c.349-2_354del
XM_011543091.3:c.349-2_354del
XM_017008919.2:c.349-2_354del
NM_005713.3:c.349-2_354del
NM_031361.3:c.349-2_354del
NM_001379002.1:c.349-2_354del
NM_001379003.1:c.349-2_354del
NM_001379004.1:c.349-2_354del
NM_001379029.1:c.349-2_354del