Canonical Allele Identifier: CA84733126

Gene: ATR

Linked Data

• dbSNP Id: rs879114264
• gnomAD v4: 3-142469267-T-G
• MyVariant Identifiers: chr3:g.142188109T>G (hg19) ; chr3:g.142469267T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469267T>G , CM000665.2:g.142469267T>G	GRCh38
NC_000003.11:g.142188109T>G , CM000665.1:g.142188109T>G	GRCh37
NC_000003.10:g.143670799T>G	NCBI36
NG_008951.1:g.114560A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6552+70A>C MANE Select	ENSP00000343741.4:n.6552+70A>C
ENST00000513291.2:n.1736+70A>C
ENST00000654170.1:n.1395+70A>C
ENST00000656590.1:c.5342+70A>C
ENST00000661310.1:c.6360+70A>C	ENSP00000499589.1:n.6360+70A>C
ENST00000665483.1:n.407+70A>C
ENST00000666447.1:n.457A>C
ENST00000666943.1:n.2086A>C
ENST00000350721.8:c.6552+70A>C	ENSP00000343741.4:n.6552+70A>C
ENST00000513291.1:c.91+70A>C
NM_001184.3:c.6552+70A>C	NP_001175.2:n.6552+70A>C
XM_011512924.1:c.6558+70A>C	XP_011511226.1:n.6558+70A>C
XM_011512925.1:c.6366+70A>C	XP_011511227.1:n.6366+70A>C
XR_924147.1:n.6647+70A>C
XR_924148.1:n.6647+70A>C
XR_924149.1:n.6526+70A>C
NM_001354579.1:c.6360+70A>C	NP_001341508.1:n.6360+70A>C
XR_001740179.2:n.6641+70A>C
XR_924148.2:n.6647+70A>C
NM_001184.4:c.6552+70A>C MANE Select	NP_001175.2:n.6552+70A>C
NM_001354579.2:c.6360+70A>C	NP_001341508.1:n.6360+70A>C