Canonical Allele Identifier: CA12056203

Gene: ATG10

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.82242227T>A , CM000667.2:g.82242227T>A	GRCh38
NC_000005.9:g.81538046T>A , CM000667.1:g.81538046T>A	GRCh37
NC_000005.8:g.81573802T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282185.8:c.454-10335T>A MANE Select	ENSP00000282185.3:n.454-10335T>A
ENST00000282185.7:c.454-10335T>A	ENSP00000282185.3:n.454-10335T>A
ENST00000458350.7:c.454-10335T>A	ENSP00000404938.3:n.454-10335T>A
ENST00000504770.5:c.454-570T>A	ENSP00000424236.1:n.454-570T>A
ENST00000508814.5:n.163-10335T>A
ENST00000513634.1:c.454-10335T>A	ENSP00000425225.1:n.454-10335T>A
ENST00000514253.2:n.192-33918T>A
NM_001131028.1:c.454-10335T>A	NP_001124500.1:n.454-10335T>A
NM_031482.4:c.454-10335T>A	NP_113670.1:n.454-10335T>A
XM_005248610.3:c.454-10335T>A	XP_005248667.1:n.454-10335T>A
XM_005248611.3:c.454-10335T>A	XP_005248668.1:n.454-10335T>A
XM_005248612.2:c.346-10335T>A	XP_005248669.1:n.346-10335T>A
XM_011543660.1:c.328-10335T>A	XP_011541962.1:n.328-10335T>A
XM_011543661.1:c.244-10335T>A	XP_011541963.1:n.244-10335T>A
XM_005248610.5:c.454-10335T>A	XP_005248667.1:n.454-10335T>A
XM_005248611.5:c.454-10335T>A	XP_005248668.1:n.454-10335T>A
XM_005248612.3:c.346-10335T>A	XP_005248669.1:n.346-10335T>A
XM_011543660.2:c.328-10335T>A	XP_011541962.1:n.328-10335T>A
XM_011543661.2:c.244-10335T>A	XP_011541963.1:n.244-10335T>A
XM_017009944.1:c.346-10335T>A	XP_016865433.1:n.346-10335T>A
NM_031482.5:c.454-10335T>A MANE Select	NP_113670.1:n.454-10335T>A
NM_001131028.2:c.454-10335T>A	NP_001124500.1:n.454-10335T>A