Canonical Allele Identifier: CA899875262

Gene: ATR

Linked Data

• dbSNP Id: rs1477868167
• gnomAD v3: 3-142469925-T-A
• gnomAD v4: 3-142469925-T-A
• MyVariant Identifiers: chr3:g.142188767T>A (hg19) ; chr3:g.142469925T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469925T>A , CM000665.2:g.142469925T>A	GRCh38
NC_000003.11:g.142188767T>A , CM000665.1:g.142188767T>A	GRCh37
NC_000003.10:g.143671457T>A	NCBI36
NG_008951.1:g.113902A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6319+161A>T MANE Select	ENSP00000343741.4:n.6319+161A>T
ENST00000513291.2:n.1503+161A>T
ENST00000654170.1:n.1162+161A>T
ENST00000656590.1:c.5109+161A>T
ENST00000661310.1:c.6127+161A>T	ENSP00000499589.1:n.6127+161A>T
ENST00000665483.1:n.174+161A>T
ENST00000666447.1:n.154+161A>T
ENST00000666943.1:n.1783+161A>T
ENST00000350721.8:c.6319+161A>T	ENSP00000343741.4:n.6319+161A>T
NM_001184.3:c.6319+161A>T	NP_001175.2:n.6319+161A>T
XM_011512924.1:c.6325+161A>T	XP_011511226.1:n.6325+161A>T
XM_011512925.1:c.6133+161A>T	XP_011511227.1:n.6133+161A>T
XR_924147.1:n.6414+161A>T
XR_924148.1:n.6414+161A>T
XR_924149.1:n.6293+161A>T
NM_001354579.1:c.6127+161A>T	NP_001341508.1:n.6127+161A>T
XR_001740179.2:n.6408+161A>T
XR_001740180.2:n.6462+161A>T
XR_001740181.2:n.6341+161A>T
XR_001740182.1:n.6293+161A>T
XR_002959543.1:n.6518+161A>T
XR_924148.2:n.6414+161A>T
NM_001184.4:c.6319+161A>T MANE Select	NP_001175.2:n.6319+161A>T
NM_001354579.2:c.6127+161A>T	NP_001341508.1:n.6127+161A>T