Canonical Allele Identifier: CA2516913129

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142498085_142498086insG , CM000665.2:g.142498085_142498086insG	GRCh38
NC_000003.11:g.142216927_142216928insG , CM000665.1:g.142216927_142216928insG	GRCh37
NC_000003.10:g.143699617_143699618insG	NCBI36
NG_008951.1:g.85741_85742insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.5558+511_5558+512insC MANE Select	ENSP00000343741.4:n.5558+511_5558+512insC...
ENST00000513291.2:n.742+511_742+512insC
ENST00000653868.1:n.5587+511_5587+512insC
ENST00000656590.1:c.4348+511_4348+512insC
ENST00000661310.1:c.5366+511_5366+512insC	ENSP00000499589.1:n.5366+511_5366+512insC...
ENST00000666943.1:n.1022+511_1022+512insC
ENST00000350721.8:c.5558+511_5558+512insC	ENSP00000343741.4:n.5558+511_5558+512insC...
ENST00000507620.2:n.654+511_654+512insC
ENST00000514393.5:n.241+511_241+512insC
NM_001184.3:c.5558+511_5558+512insC	NP_001175.2:n.5558+511_5558+512insC
XM_011512924.1:c.5564+511_5564+512insC	XP_011511226.1:n.5564+511_5564+512insC
XM_011512925.1:c.5372+511_5372+512insC	XP_011511227.1:n.5372+511_5372+512insC
XM_011512926.1:c.5564+511_5564+512insC	XP_011511228.1:n.5564+511_5564+512insC
XM_011512927.1:c.5564+511_5564+512insC	XP_011511229.1:n.5564+511_5564+512insC
XR_924147.1:n.5653+511_5653+512insC
XR_924148.1:n.5653+511_5653+512insC
XR_924149.1:n.5653+511_5653+512insC
NM_001354579.1:c.5366+511_5366+512insC	NP_001341508.1:n.5366+511_5366+512insC
XR_001740179.2:n.5647+511_5647+512insC
XR_001740180.2:n.5653+511_5653+512insC
XR_001740181.2:n.5653+511_5653+512insC
XR_001740182.1:n.5653+511_5653+512insC
XR_002959543.1:n.5653+511_5653+512insC
XR_924148.2:n.5653+511_5653+512insC
NM_001184.4:c.5558+511_5558+512insC MANE Select	NP_001175.2:n.5558+511_5558+512insC
NM_001354579.2:c.5366+511_5366+512insC	NP_001341508.1:n.5366+511_5366+512insC