Canonical Allele Identifier: CA3331361

Gene: ATG10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.82164504G>A , CM000667.2:g.82164504G>A	GRCh38
NC_000005.9:g.81460323G>A , CM000667.1:g.81460323G>A	GRCh37
NC_000005.8:g.81496079G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282185.8:c.322G>A MANE Select	ENSP00000282185.3:p.Val108Met
ENST00000282185.7:c.322G>A	ENSP00000282185.3:p.Val108Met
ENST00000458350.7:c.322G>A	ENSP00000404938.3:p.Val108Met
ENST00000504770.5:c.322G>A	ENSP00000424236.1:p.Val108Met
ENST00000508814.5:n.65-13986G>A
ENST00000513634.1:c.322G>A	ENSP00000425225.1:p.Val108Met
ENST00000514253.2:n.60G>A
NM_001131028.1:c.322G>A	NP_001124500.1:p.Val108Met
NM_031482.4:c.322G>A	NP_113670.1:p.Val108Met
XM_005248610.3:c.322G>A	XP_005248667.1:p.Val108Met
XM_005248611.3:c.322G>A	XP_005248668.1:p.Val108Met
XM_005248612.2:c.214G>A	XP_005248669.1:p.Val72Met
XM_011543660.1:c.196G>A	XP_011541962.1:p.Val66Met
XM_011543661.1:c.112G>A	XP_011541963.1:p.Val38Met
XM_005248610.5:c.322G>A	XP_005248667.1:p.Val108Met
XM_005248611.5:c.322G>A	XP_005248668.1:p.Val108Met
XM_005248612.3:c.214G>A	XP_005248669.1:p.Val72Met
XM_011543660.2:c.196G>A	XP_011541962.1:p.Val66Met
XM_011543661.2:c.112G>A	XP_011541963.1:p.Val38Met
XM_017009944.1:c.214G>A	XP_016865433.1:p.Val72Met
NM_031482.5:c.322G>A MANE Select	NP_113670.1:p.Val108Met
NM_001131028.2:c.322G>A	NP_001124500.1:p.Val108Met