Canonical Allele Identifier: CA2758700083

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470205_142470206insAACCAAACACACCCAACA , CM000665.2:g.142470205_142470206insAACCAAACACACCCAACA	GRCh38
NC_000003.11:g.142189047_142189048insAACCAAACACACCCAACA , CM000665.1:g.142189047_142189048insAACCAAACACACCCAACA	GRCh37
NC_000003.10:g.143671737_143671738insAACCAAACACACCCAACA	NCBI36
NG_008951.1:g.113622_113623insGTTGGGTGTGTTTGGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6222-22_6222-21insGTTGGGTGTGTTTGGTTT MANE Select	ENSP00000343741.4:n.6222-22_6222-21insGTTGGGTGTGTTTGGTTT
ENST00000513291.2:n.1406-22_1406-21insGTTGGGTGTGTTTGGTTT
ENST00000654170.1:n.1065-22_1065-21insGTTGGGTGTGTTTGGTTT
ENST00000656590.1:c.5012-22_5012-21insGTTGGGTGTGTTTGGTTT
ENST00000661310.1:c.6030-22_6030-21insGTTGGGTGTGTTTGGTTT	ENSP00000499589.1:n.6030-22_6030-21insGTTGGGTGTGTTTGGTTT
ENST00000665483.1:n.77-22_77-21insGTTGGGTGTGTTTGGTTT
ENST00000666447.1:n.57-22_57-21insGTTGGGTGTGTTTGGTTT
ENST00000666943.1:n.1686-22_1686-21insGTTGGGTGTGTTTGGTTT
ENST00000350721.8:c.6222-22_6222-21insGTTGGGTGTGTTTGGTTT	ENSP00000343741.4:n.6222-22_6222-21insGTTGGGTGTGTTTGGTTT
NM_001184.3:c.6222-22_6222-21insGTTGGGTGTGTTTGGTTT	NP_001175.2:n.6222-22_6222-21insGTTGGGTGTGTTTGGTTT
XM_011512924.1:c.6228-22_6228-21insGTTGGGTGTGTTTGGTTT	XP_011511226.1:n.6228-22_6228-21insGTTGGGTGTGTTTGGTTT
XM_011512925.1:c.6036-22_6036-21insGTTGGGTGTGTTTGGTTT	XP_011511227.1:n.6036-22_6036-21insGTTGGGTGTGTTTGGTTT
XR_924147.1:n.6317-22_6317-21insGTTGGGTGTGTTTGGTTT
XR_924148.1:n.6317-22_6317-21insGTTGGGTGTGTTTGGTTT
XR_924149.1:n.6196-22_6196-21insGTTGGGTGTGTTTGGTTT
NM_001354579.1:c.6030-22_6030-21insGTTGGGTGTGTTTGGTTT	NP_001341508.1:n.6030-22_6030-21insGTTGGGTGTGTTTGGTTT
XR_001740179.2:n.6311-22_6311-21insGTTGGGTGTGTTTGGTTT
XR_001740180.2:n.6365-22_6365-21insGTTGGGTGTGTTTGGTTT
XR_001740181.2:n.6244-22_6244-21insGTTGGGTGTGTTTGGTTT
XR_001740182.1:n.6196-22_6196-21insGTTGGGTGTGTTTGGTTT
XR_002959543.1:n.6421-22_6421-21insGTTGGGTGTGTTTGGTTT
XR_924148.2:n.6317-22_6317-21insGTTGGGTGTGTTTGGTTT
NM_001184.4:c.6222-22_6222-21insGTTGGGTGTGTTTGGTTT MANE Select	NP_001175.2:n.6222-22_6222-21insGTTGGGTGTGTTTGGTTT
NM_001354579.2:c.6030-22_6030-21insGTTGGGTGTGTTTGGTTT	NP_001341508.1:n.6030-22_6030-21insGTTGGGTGTGTTTGGTTT