Canonical Allele Identifier: CA12203194
Gene: ATG5 HGNC NCBI

Linked Data

dbSNP Id: rs12201458

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.106194812C>A , CM000668.2:g.106194812C>A GRCh38
NC_000006.11:g.106642687C>A , CM000668.1:g.106642687C>A GRCh37
NC_000006.10:g.106749380C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000360666.6:c.*45+7160G>T ENSP00000353884.4:n.*45+7160G>T
ENST00000369076.8:c.691+7160G>T MANE Select ENSP00000358072.3:n.691+7160G>T
ENST00000635758.2:c.457+7160G>T ENSP00000490493.1:n.457+7160G>T
ENST00000636335.1:c.457+7160G>T ENSP00000490221.1:n.457+7160G>T
ENST00000636437.1:c.457+7160G>T ENSP00000490376.1:n.457+7160G>T
ENST00000646025.1:c.*127+7160G>T ENSP00000495958.1:n.*127+7160G>T
ENST00000343245.7:c.691+7160G>T ENSP00000343313.3:n.691+7160G>T
ENST00000360666.5:c.*45+7160G>T ENSP00000353884.4:n.*45+7160G>T
ENST00000369070.5:c.457+7160G>T ENSP00000358066.1:n.457+7160G>T
ENST00000369076.7:c.691+7160G>T ENSP00000358072.3:n.691+7160G>T
ENST00000475645.1:n.458+7160G>T
ENST00000613993.1:c.596+7160G>T ENSP00000483135.1:n.596+7160G>T
NM_001286106.1:c.691+7160G>T NP_001273035.1:n.691+7160G>T
NM_001286107.1:c.457+7160G>T NP_001273036.1:n.457+7160G>T
NM_001286108.1:c.*45+7160G>T NP_001273037.1:n.*45+7160G>T
NM_001286111.1:c.*45+7160G>T NP_001273040.1:n.*45+7160G>T
NM_004849.3:c.691+7160G>T NP_004840.1:n.691+7160G>T
NR_104402.1:n.654+7160G>T
NR_104403.1:n.526+7160G>T
XM_024446590.1:c.457+7160G>T XP_024302358.1:n.457+7160G>T
XR_001743757.2:n.1151+7160G>T
NM_004849.4:c.691+7160G>T MANE Select NP_004840.1:n.691+7160G>T
NM_001286106.2:c.691+7160G>T NP_001273035.1:n.691+7160G>T
NM_001286107.2:c.457+7160G>T NP_001273036.1:n.457+7160G>T
NM_001286108.2:c.*45+7160G>T NP_001273037.1:n.*45+7160G>T
NM_001286111.2:c.*45+7160G>T NP_001273040.1:n.*45+7160G>T