Canonical Allele Identifier: CA84733772

Gene: ATR

Linked Data

• dbSNP Id: rs770741568
• MyVariant Identifiers: chr3:g.142470065C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470065C>T , CM000665.2:g.142470065C>T	GRCh38
NC_000003.11:g.142188907C>T , CM000665.1:g.142188907C>T	GRCh37
NC_000003.10:g.143671597C>T	NCBI36
NG_008951.1:g.113762G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6319+21G>A MANE Select	ENSP00000343741.4:n.6319+21G>A
ENST00000513291.2:n.1503+21G>A
ENST00000654170.1:n.1162+21G>A
ENST00000656590.1:c.5109+21G>A
ENST00000661310.1:c.6127+21G>A	ENSP00000499589.1:n.6127+21G>A
ENST00000665483.1:n.174+21G>A
ENST00000666447.1:n.154+21G>A
ENST00000666943.1:n.1783+21G>A
ENST00000350721.8:c.6319+21G>A	ENSP00000343741.4:n.6319+21G>A
NM_001184.3:c.6319+21G>A	NP_001175.2:n.6319+21G>A
XM_011512924.1:c.6325+21G>A	XP_011511226.1:n.6325+21G>A
XM_011512925.1:c.6133+21G>A	XP_011511227.1:n.6133+21G>A
XR_924147.1:n.6414+21G>A
XR_924148.1:n.6414+21G>A
XR_924149.1:n.6293+21G>A
NM_001354579.1:c.6127+21G>A	NP_001341508.1:n.6127+21G>A
XR_001740179.2:n.6408+21G>A
XR_001740180.2:n.6462+21G>A
XR_001740181.2:n.6341+21G>A
XR_001740182.1:n.6293+21G>A
XR_002959543.1:n.6518+21G>A
XR_924148.2:n.6414+21G>A
NM_001184.4:c.6319+21G>A MANE Select	NP_001175.2:n.6319+21G>A
NM_001354579.2:c.6127+21G>A	NP_001341508.1:n.6127+21G>A