Canonical Allele Identifier: CA2704289105

Gene: ATR

Linked Data

• dbSNP Id: rs2108280494

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469953C>T , CM000665.2:g.142469953C>T	GRCh38
NC_000003.11:g.142188795C>T , CM000665.1:g.142188795C>T	GRCh37
NC_000003.10:g.143671485C>T	NCBI36
NG_008951.1:g.113874G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6319+133G>A MANE Select	ENSP00000343741.4:n.6319+133G>A
ENST00000513291.2:n.1503+133G>A
ENST00000654170.1:n.1162+133G>A
ENST00000656590.1:c.5109+133G>A
ENST00000661310.1:c.6127+133G>A	ENSP00000499589.1:n.6127+133G>A
ENST00000665483.1:n.174+133G>A
ENST00000666447.1:n.154+133G>A
ENST00000666943.1:n.1783+133G>A
ENST00000350721.8:c.6319+133G>A	ENSP00000343741.4:n.6319+133G>A
NM_001184.3:c.6319+133G>A	NP_001175.2:n.6319+133G>A
XM_011512924.1:c.6325+133G>A	XP_011511226.1:n.6325+133G>A
XM_011512925.1:c.6133+133G>A	XP_011511227.1:n.6133+133G>A
XR_924147.1:n.6414+133G>A
XR_924148.1:n.6414+133G>A
XR_924149.1:n.6293+133G>A
NM_001354579.1:c.6127+133G>A	NP_001341508.1:n.6127+133G>A
XR_001740179.2:n.6408+133G>A
XR_001740180.2:n.6462+133G>A
XR_001740181.2:n.6341+133G>A
XR_001740182.1:n.6293+133G>A
XR_002959543.1:n.6518+133G>A
XR_924148.2:n.6414+133G>A
NM_001184.4:c.6319+133G>A MANE Select	NP_001175.2:n.6319+133G>A
NM_001354579.2:c.6127+133G>A	NP_001341508.1:n.6127+133G>A