Canonical Allele Identifier: CA899892416

Gene: ATR

Linked Data

• dbSNP Id: rs1365965913
• gnomAD v3: 3-142498082-T-G
• gnomAD v4: 3-142498082-T-G
• MyVariant Identifiers: chr3:g.142216924T>G (hg19) ; chr3:g.142498082T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142498082T>G , CM000665.2:g.142498082T>G	GRCh38
NC_000003.11:g.142216924T>G , CM000665.1:g.142216924T>G	GRCh37
NC_000003.10:g.143699614T>G	NCBI36
NG_008951.1:g.85745A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.5558+515A>C MANE Select	ENSP00000343741.4:n.5558+515A>C
ENST00000513291.2:n.742+515A>C
ENST00000653868.1:n.5587+515A>C
ENST00000656590.1:c.4348+515A>C
ENST00000661310.1:c.5366+515A>C	ENSP00000499589.1:n.5366+515A>C
ENST00000666943.1:n.1022+515A>C
ENST00000350721.8:c.5558+515A>C	ENSP00000343741.4:n.5558+515A>C
ENST00000507620.2:n.654+515A>C
ENST00000514393.5:n.241+515A>C
NM_001184.3:c.5558+515A>C	NP_001175.2:n.5558+515A>C
XM_011512924.1:c.5564+515A>C	XP_011511226.1:n.5564+515A>C
XM_011512925.1:c.5372+515A>C	XP_011511227.1:n.5372+515A>C
XM_011512926.1:c.5564+515A>C	XP_011511228.1:n.5564+515A>C
XM_011512927.1:c.5564+515A>C	XP_011511229.1:n.5564+515A>C
XR_924147.1:n.5653+515A>C
XR_924148.1:n.5653+515A>C
XR_924149.1:n.5653+515A>C
NM_001354579.1:c.5366+515A>C	NP_001341508.1:n.5366+515A>C
XR_001740179.2:n.5647+515A>C
XR_001740180.2:n.5653+515A>C
XR_001740181.2:n.5653+515A>C
XR_001740182.1:n.5653+515A>C
XR_002959543.1:n.5653+515A>C
XR_924148.2:n.5653+515A>C
NM_001184.4:c.5558+515A>C MANE Select	NP_001175.2:n.5558+515A>C
NM_001354579.2:c.5366+515A>C	NP_001341508.1:n.5366+515A>C