Canonical Allele Identifier: CA1653351507

Gene: ATG5

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.106316991G>C , CM000668.2:g.106316991G>C	GRCh38
NC_000006.11:g.106764866G>C , CM000668.1:g.106764866G>C	GRCh37
NC_000006.10:g.106871559G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360666.6:c.-58-725C>G	ENSP00000353884.4:n.-58-725C>G
ENST00000369076.8:c.-58-725C>G MANE Select	ENSP00000358072.3:n.-58-725C>G
ENST00000635758.2:c.-164-725C>G	ENSP00000490493.1:n.-164-725C>G
ENST00000636335.1:c.-164-725C>G	ENSP00000490221.1:n.-164-725C>G
ENST00000636437.1:c.-164-725C>G	ENSP00000490376.1:n.-164-725C>G
ENST00000646025.1:c.-58-725C>G	ENSP00000495958.1:n.-58-725C>G
ENST00000343245.7:c.-58-725C>G	ENSP00000343313.3:n.-58-725C>G
ENST00000360666.5:c.-58-725C>G	ENSP00000353884.4:n.-58-725C>G
ENST00000369070.5:c.-164-725C>G	ENSP00000358066.1:n.-164-725C>G
ENST00000369076.7:c.-58-725C>G	ENSP00000358072.3:n.-58-725C>G
NM_001286106.1:c.-58-725C>G	NP_001273035.1:n.-58-725C>G
NM_001286107.1:c.-164-725C>G	NP_001273036.1:n.-164-725C>G
NM_001286108.1:c.-58-725C>G	NP_001273037.1:n.-58-725C>G
NM_001286111.1:c.-58-725C>G	NP_001273040.1:n.-58-725C>G
NM_004849.3:c.-58-725C>G	NP_004840.1:n.-58-725C>G
XM_011536263.1:c.-58-725C>G	XP_011534565.1:n.-58-725C>G
XM_024446590.1:c.-164-725C>G	XP_024302358.1:n.-164-725C>G
XR_001743757.2:n.265-725C>G
NM_004849.4:c.-58-725C>G MANE Select	NP_004840.1:n.-58-725C>G
NM_001286106.2:c.-58-725C>G	NP_001273035.1:n.-58-725C>G
NM_001286107.2:c.-164-725C>G	NP_001273036.1:n.-164-725C>G
NM_001286108.2:c.-58-725C>G	NP_001273037.1:n.-58-725C>G
NM_001286111.2:c.-58-725C>G	NP_001273040.1:n.-58-725C>G