Canonical Allele Identifier: CA360352295

Gene: ATG10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.82178490A>G , CM000667.2:g.82178490A>G	GRCh38
NC_000005.9:g.81474309A>G , CM000667.1:g.81474309A>G	GRCh37
NC_000005.8:g.81510065A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282185.8:c.356A>G MANE Select	ENSP00000282185.3:p.Asp119Gly
ENST00000282185.7:c.356A>G	ENSP00000282185.3:p.Asp119Gly
ENST00000458350.7:c.356A>G	ENSP00000404938.3:p.Asp119Gly
ENST00000504770.5:c.356A>G	ENSP00000424236.1:p.Asp119Gly
ENST00000508814.5:n.65A>G
ENST00000513634.1:c.356A>G	ENSP00000425225.1:p.Asp119Gly
ENST00000514253.2:n.94A>G
NM_001131028.1:c.356A>G	NP_001124500.1:p.Asp119Gly
NM_031482.4:c.356A>G	NP_113670.1:p.Asp119Gly
XM_005248610.3:c.356A>G	XP_005248667.1:p.Asp119Gly
XM_005248611.3:c.356A>G	XP_005248668.1:p.Asp119Gly
XM_005248612.2:c.248A>G	XP_005248669.1:p.Asp83Gly
XM_011543660.1:c.230A>G	XP_011541962.1:p.Asp77Gly
XM_011543661.1:c.146A>G	XP_011541963.1:p.Asp49Gly
XM_005248610.5:c.356A>G	XP_005248667.1:p.Asp119Gly
XM_005248611.5:c.356A>G	XP_005248668.1:p.Asp119Gly
XM_005248612.3:c.248A>G	XP_005248669.1:p.Asp83Gly
XM_011543660.2:c.230A>G	XP_011541962.1:p.Asp77Gly
XM_011543661.2:c.146A>G	XP_011541963.1:p.Asp49Gly
XM_017009944.1:c.248A>G	XP_016865433.1:p.Asp83Gly
NM_031482.5:c.356A>G MANE Select	NP_113670.1:p.Asp119Gly
NM_001131028.2:c.356A>G	NP_001124500.1:p.Asp119Gly