Canonical Allele Identifier: CA1556119793

Gene: CERT1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75426530_75426531delinsGA , CM000667.2:g.75426530_75426531delinsGA	GRCh38
NC_000005.9:g.74722355_74722356delinsGA , CM000667.1:g.74722355_74722356delinsGA	GRCh37
NC_000005.8:g.74758111_74758112delinsGA	NCBI36
NG_029492.1:g.90451_90452delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647512.2:n.779-53_779-52delinsTC
ENST00000261415.12:c.349-53_349-52delinsTC	ENSP00000261415.8:n.349-53_349-52delinsTC
ENST00000380494.10:c.141-53_141-52delinsTC
ENST00000405807.10:c.733-53_733-52delinsTC	ENSP00000383996.4:n.733-53_733-52delinsTC
ENST00000642225.1:c.349-53_349-52delinsTC	ENSP00000493604.1:n.349-53_349-52delinsTC
ENST00000642556.1:c.349-53_349-52delinsTC	ENSP00000496016.1:n.349-53_349-52delinsTC
ENST00000642809.1:c.349-53_349-52delinsTC	ENSP00000494804.1:n.349-53_349-52delinsTC
ENST00000643158.1:c.349-53_349-52delinsTC	ENSP00000496462.1:n.349-53_349-52delinsTC
ENST00000643773.1:c.-48-53_-48-52delinsTC	ENSP00000493565.1:n.-48-53_-48-52delinsTC
ENST00000643780.2:c.349-53_349-52delinsTC MANE Select	ENSP00000495760.1:n.349-53_349-52delinsTC
ENST00000644072.2:c.349-53_349-52delinsTC	ENSP00000494110.2:n.349-53_349-52delinsTC
ENST00000644377.1:c.349-53_349-52delinsTC	ENSP00000494810.1:n.349-53_349-52delinsTC
ENST00000644445.1:c.349-53_349-52delinsTC	ENSP00000496243.1:n.349-53_349-52delinsTC
ENST00000644516.1:c.349-53_349-52delinsTC	ENSP00000495430.1:n.349-53_349-52delinsTC
ENST00000644912.1:c.349-53_349-52delinsTC	ENSP00000495172.1:n.349-53_349-52delinsTC
ENST00000645483.1:c.349-53_349-52delinsTC	ENSP00000493563.1:n.349-53_349-52delinsTC
ENST00000645866.1:c.349-53_349-52delinsTC	ENSP00000494424.1:n.349-53_349-52delinsTC
ENST00000646302.1:c.349-53_349-52delinsTC	ENSP00000496472.1:n.349-53_349-52delinsTC
ENST00000646511.1:c.349-53_349-52delinsTC	ENSP00000495446.1:n.349-53_349-52delinsTC
ENST00000646713.1:c.349-53_349-52delinsTC	ENSP00000494968.1:n.349-53_349-52delinsTC
ENST00000647512.1:n.562-53_562-52delinsTC
ENST00000261415.11:c.349-53_349-52delinsTC	ENSP00000261415.7:n.349-53_349-52delinsTC
ENST00000380494.9:c.733-53_733-52delinsTC	ENSP00000369862.4:n.733-53_733-52delinsTC
ENST00000405807.8:c.349-53_349-52delinsTC	ENSP00000383996.3:n.349-53_349-52delinsTC
NM_001130105.1:c.733-53_733-52delinsTC	NP_001123577.1:n.733-53_733-52delinsTC
NM_005713.2:c.349-53_349-52delinsTC	NP_005704.1:n.349-53_349-52delinsTC
NM_031361.2:c.349-53_349-52delinsTC	NP_112729.1:n.349-53_349-52delinsTC
XM_006714513.1:c.349-53_349-52delinsTC	XP_006714576.1:n.349-53_349-52delinsTC
XM_011543090.1:c.349-53_349-52delinsTC	XP_011541392.1:n.349-53_349-52delinsTC
XM_011543091.1:c.349-53_349-52delinsTC	XP_011541393.1:n.349-53_349-52delinsTC
XM_006714513.3:c.349-53_349-52delinsTC	XP_006714576.1:n.349-53_349-52delinsTC
XM_011543090.3:c.349-53_349-52delinsTC	XP_011541392.1:n.349-53_349-52delinsTC
XM_011543091.3:c.349-53_349-52delinsTC	XP_011541393.1:n.349-53_349-52delinsTC
XM_017008919.2:c.349-53_349-52delinsTC	XP_016864408.1:n.349-53_349-52delinsTC
NM_005713.3:c.349-53_349-52delinsTC	NP_005704.1:n.349-53_349-52delinsTC
NM_031361.3:c.349-53_349-52delinsTC	NP_112729.1:n.349-53_349-52delinsTC
NM_001379002.1:c.349-53_349-52delinsTC	NP_001365931.1:n.349-53_349-52delinsTC
NM_001379003.1:c.349-53_349-52delinsTC	NP_001365932.1:n.349-53_349-52delinsTC
NM_001379004.1:c.349-53_349-52delinsTC	NP_001365933.1:n.349-53_349-52delinsTC
NM_001379029.1:c.349-53_349-52delinsTC MANE Select	NP_001365958.1:n.349-53_349-52delinsTC