Canonical Allele Identifier: CA11935188

Gene: ATG10

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.82011593C>T , CM000667.2:g.82011593C>T	GRCh38
NC_000005.9:g.81307412C>T , CM000667.1:g.81307412C>T	GRCh37
NC_000005.8:g.81343168C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282185.8:c.108+23915C>T MANE Select	ENSP00000282185.3:n.108+23915C>T
ENST00000282185.7:c.108+23915C>T	ENSP00000282185.3:n.108+23915C>T
ENST00000355178.8:c.108+23915C>T	ENSP00000347309.4:n.108+23915C>T
ENST00000458350.7:c.108+23915C>T	ENSP00000404938.3:n.108+23915C>T
ENST00000504770.5:c.108+23915C>T	ENSP00000424236.1:n.108+23915C>T
ENST00000513443.5:c.108+23915C>T	ENSP00000425182.1:n.108+23915C>T
ENST00000513634.1:c.108+23915C>T	ENSP00000425225.1:n.108+23915C>T
NM_001131028.1:c.108+23915C>T	NP_001124500.1:n.108+23915C>T
NM_031482.4:c.108+23915C>T	NP_113670.1:n.108+23915C>T
XM_005248610.3:c.108+23915C>T	XP_005248667.1:n.108+23915C>T
XM_005248611.3:c.108+23915C>T	XP_005248668.1:n.108+23915C>T
XM_005248612.2:c.108+23915C>T	XP_005248669.1:n.108+23915C>T
XM_005248610.5:c.108+23915C>T	XP_005248667.1:n.108+23915C>T
XM_005248611.5:c.108+23915C>T	XP_005248668.1:n.108+23915C>T
XM_005248612.3:c.108+23915C>T	XP_005248669.1:n.108+23915C>T
XM_017009944.1:c.108+23915C>T	XP_016865433.1:n.108+23915C>T
NM_031482.5:c.108+23915C>T MANE Select	NP_113670.1:n.108+23915C>T
NM_001131028.2:c.108+23915C>T	NP_001124500.1:n.108+23915C>T