Canonical Allele Identifier: CA354796938

Gene: ATR

Linked Data

• dbSNP Id: rs2032701774
• gnomAD v3: 3-142513572-C-T
• gnomAD v4: 3-142513572-C-T
• MyVariant Identifiers: chr3:g.142232414C>T (hg19) ; chr3:g.142513572C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513572C>T , CM000665.2:g.142513572C>T	GRCh38
NC_000003.11:g.142232414C>T , CM000665.1:g.142232414C>T	GRCh37
NC_000003.10:g.143715104C>T	NCBI36
NG_008951.1:g.70255G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4570G>A MANE Select	ENSP00000343741.4:p.Val1524Met
ENST00000653868.1:n.4599G>A
ENST00000656590.1:c.3360G>A
ENST00000661310.1:c.4378G>A	ENSP00000499589.1:p.Val1460Met
ENST00000666943.1:n.34G>A
ENST00000350721.8:c.4570G>A	ENSP00000343741.4:p.Val1524Met
NM_001184.3:c.4570G>A	NP_001175.2:p.Val1524Met
XM_011512924.1:c.4576G>A	XP_011511226.1:p.Val1526Met
XM_011512925.1:c.4384G>A	XP_011511227.1:p.Val1462Met
XM_011512926.1:c.4576G>A	XP_011511228.1:p.Val1526Met
XM_011512927.1:c.4576G>A	XP_011511229.1:p.Val1526Met
XR_924147.1:n.4665G>A
XR_924148.1:n.4665G>A
XR_924149.1:n.4665G>A
NM_001354579.1:c.4378G>A	NP_001341508.1:p.Val1460Met
XR_001740179.2:n.4659G>A
XR_001740180.2:n.4665G>A
XR_001740181.2:n.4665G>A
XR_001740182.1:n.4665G>A
XR_002959543.1:n.4665G>A
XR_924148.2:n.4665G>A
NM_001184.4:c.4570G>A MANE Select	NP_001175.2:p.Val1524Met
NM_001354579.2:c.4378G>A	NP_001341508.1:p.Val1460Met