Canonical Allele Identifier: CA813968890
Gene: CERT1 HGNC NCBI

Linked Data

dbSNP Id: rs1217416677
gnomAD v4: 5-75426561-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.75426561G>T , CM000667.2:g.75426561G>T GRCh38
NC_000005.9:g.74722386G>T , CM000667.1:g.74722386G>T GRCh37
NC_000005.8:g.74758142G>T NCBI36
NG_029492.1:g.90421C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647512.2:n.779-83C>A
ENST00000261415.12:c.349-83C>A ENSP00000261415.8:n.349-83C>A
ENST00000380494.10:c.141-83C>A
ENST00000405807.10:c.733-83C>A ENSP00000383996.4:n.733-83C>A
ENST00000642225.1:c.349-83C>A ENSP00000493604.1:n.349-83C>A
ENST00000642556.1:c.349-83C>A ENSP00000496016.1:n.349-83C>A
ENST00000642809.1:c.349-83C>A ENSP00000494804.1:n.349-83C>A
ENST00000643158.1:c.349-83C>A ENSP00000496462.1:n.349-83C>A
ENST00000643773.1:c.-48-83C>A ENSP00000493565.1:n.-48-83C>A
ENST00000643780.2:c.349-83C>A MANE Select ENSP00000495760.1:n.349-83C>A
ENST00000644072.2:c.349-83C>A ENSP00000494110.2:n.349-83C>A
ENST00000644377.1:c.349-83C>A ENSP00000494810.1:n.349-83C>A
ENST00000644445.1:c.349-83C>A ENSP00000496243.1:n.349-83C>A
ENST00000644516.1:c.349-83C>A ENSP00000495430.1:n.349-83C>A
ENST00000644912.1:c.349-83C>A ENSP00000495172.1:n.349-83C>A
ENST00000645483.1:c.349-83C>A ENSP00000493563.1:n.349-83C>A
ENST00000645866.1:c.349-83C>A ENSP00000494424.1:n.349-83C>A
ENST00000646302.1:c.349-83C>A ENSP00000496472.1:n.349-83C>A
ENST00000646511.1:c.349-83C>A ENSP00000495446.1:n.349-83C>A
ENST00000646713.1:c.349-83C>A ENSP00000494968.1:n.349-83C>A
ENST00000647512.1:n.562-83C>A
ENST00000261415.11:c.349-83C>A ENSP00000261415.7:n.349-83C>A
ENST00000380494.9:c.733-83C>A ENSP00000369862.4:n.733-83C>A
ENST00000405807.8:c.349-83C>A ENSP00000383996.3:n.349-83C>A
NM_001130105.1:c.733-83C>A NP_001123577.1:n.733-83C>A
NM_005713.2:c.349-83C>A NP_005704.1:n.349-83C>A
NM_031361.2:c.349-83C>A NP_112729.1:n.349-83C>A
XM_006714513.1:c.349-83C>A XP_006714576.1:n.349-83C>A
XM_011543090.1:c.349-83C>A XP_011541392.1:n.349-83C>A
XM_011543091.1:c.349-83C>A XP_011541393.1:n.349-83C>A
XM_006714513.3:c.349-83C>A XP_006714576.1:n.349-83C>A
XM_011543090.3:c.349-83C>A XP_011541392.1:n.349-83C>A
XM_011543091.3:c.349-83C>A XP_011541393.1:n.349-83C>A
XM_017008919.2:c.349-83C>A XP_016864408.1:n.349-83C>A
NM_005713.3:c.349-83C>A NP_005704.1:n.349-83C>A
NM_031361.3:c.349-83C>A NP_112729.1:n.349-83C>A
NM_001379002.1:c.349-83C>A NP_001365931.1:n.349-83C>A
NM_001379003.1:c.349-83C>A NP_001365932.1:n.349-83C>A
NM_001379004.1:c.349-83C>A NP_001365933.1:n.349-83C>A
NM_001379029.1:c.349-83C>A MANE Select NP_001365958.1:n.349-83C>A