Canonical Allele Identifier: CA1407006781

Gene: ATR

Linked Data

• dbSNP Id: rs2031756730

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142498229dup , CM000665.2:g.142498229dup	GRCh38
NC_000003.11:g.142217071dup , CM000665.1:g.142217071dup	GRCh37
NC_000003.10:g.143699761dup	NCBI36
NG_008951.1:g.85603dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.5558+373dup MANE Select	ENSP00000343741.4:n.5558+373dup
ENST00000513291.2:n.742+373dup
ENST00000653868.1:n.5587+373dup
ENST00000656590.1:c.4348+373dup
ENST00000661310.1:c.5366+373dup	ENSP00000499589.1:n.5366+373dup
ENST00000666943.1:n.1022+373dup
ENST00000350721.8:c.5558+373dup	ENSP00000343741.4:n.5558+373dup
ENST00000507620.2:n.654+373dup
ENST00000514393.5:n.241+373dup
NM_001184.3:c.5558+373dup	NP_001175.2:n.5558+373dup
XM_011512924.1:c.5564+373dup	XP_011511226.1:n.5564+373dup
XM_011512925.1:c.5372+373dup	XP_011511227.1:n.5372+373dup
XM_011512926.1:c.5564+373dup	XP_011511228.1:n.5564+373dup
XM_011512927.1:c.5564+373dup	XP_011511229.1:n.5564+373dup
XR_924147.1:n.5653+373dup
XR_924148.1:n.5653+373dup
XR_924149.1:n.5653+373dup
NM_001354579.1:c.5366+373dup	NP_001341508.1:n.5366+373dup
XR_001740179.2:n.5647+373dup
XR_001740180.2:n.5653+373dup
XR_001740181.2:n.5653+373dup
XR_001740182.1:n.5653+373dup
XR_002959543.1:n.5653+373dup
XR_924148.2:n.5653+373dup
NM_001184.4:c.5558+373dup MANE Select	NP_001175.2:n.5558+373dup
NM_001354579.2:c.5366+373dup	NP_001341508.1:n.5366+373dup