Canonical Allele Identifier: CA3331468

Gene: ATG10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.82253397C>T , CM000667.2:g.82253397C>T	GRCh38
NC_000005.9:g.81549216C>T , CM000667.1:g.81549216C>T	GRCh37
NC_000005.8:g.81584972C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_031482.5:c.635C>T MANE Select	NP_113670.1:p.Thr212Met
ENST00000282185.8:c.635C>T MANE Select	ENSP00000282185.3:p.Thr212Met
NM_001131028.1:c.635C>T	NP_001124500.1:p.Thr212Met
NM_001131028.2:c.635C>T	NP_001124500.1:p.Thr212Met
NM_031482.4:c.635C>T	NP_113670.1:p.Thr212Met
ENST00000282185.7:c.635C>T	ENSP00000282185.3:p.Thr212Met
ENST00000458350.7:c.635C>T	ENSP00000404938.3:p.Thr212Met
ENST00000504770.5:c.*205C>T	ENSP00000424236.1:n.*205C>T
ENST00000508814.5:n.260+738C>T
ENST00000514253.2:n.192-22748C>T
XM_005248610.3:c.635C>T	XP_005248667.1:p.Thr212Met
XM_005248610.5:c.635C>T	XP_005248667.1:p.Thr212Met
XM_005248611.3:c.635C>T	XP_005248668.1:p.Thr212Met
XM_005248611.5:c.635C>T	XP_005248668.1:p.Thr212Met
XM_005248612.2:c.527C>T	XP_005248669.1:p.Thr176Met
XM_005248612.3:c.527C>T	XP_005248669.1:p.Thr176Met
XM_011543660.1:c.509C>T	XP_011541962.1:p.Thr170Met
XM_011543660.2:c.509C>T	XP_011541962.1:p.Thr170Met
XM_011543661.1:c.425C>T	XP_011541963.1:p.Thr142Met
XM_011543661.2:c.425C>T	XP_011541963.1:p.Thr142Met
XM_017009944.1:c.527C>T	XP_016865433.1:p.Thr176Met