Canonical Allele Identifier: CA436172648

Gene: ATR

Linked Data

• ClinVar Variation Id: 1761386
• ClinVar RCV Id: RCV002416888 ; RCV003099802
• dbSNP Id: rs1437603790
• gnomAD v2: 3-142281449-T-C
• gnomAD v3: 3-142562607-T-C
• gnomAD v4: 3-142562607-T-C
• MyVariant Identifiers: chr3:g.142281449T>C (hg19) ; chr3:g.142562607T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142562607T>C , CM000665.2:g.142562607T>C	GRCh38
NC_000003.11:g.142281449T>C , CM000665.1:g.142281449T>C	GRCh37
NC_000003.10:g.143764139T>C	NCBI36
NG_008951.1:g.21220A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.795A>G MANE Select	ENSP00000343741.4:p.Pro265=
ENST00000515149.3:c.293-1186A>G	ENSP00000425897.3:n.293-1186A>G
ENST00000653868.1:n.824A>G
ENST00000657914.1:n.3153A>G
ENST00000659195.1:n.2860A>G
ENST00000661310.1:c.795A>G	ENSP00000499589.1:p.Pro265=
ENST00000350721.8:c.795A>G	ENSP00000343741.4:p.Pro265=
ENST00000507148.1:c.293-259A>G	ENSP00000426595.1:n.293-259A>G
NM_001184.3:c.795A>G	NP_001175.2:p.Pro265=
XM_011512924.1:c.795A>G	XP_011511226.1:p.Pro265=
XM_011512925.1:c.795A>G	XP_011511227.1:p.Pro265=
XM_011512926.1:c.795A>G	XP_011511228.1:p.Pro265=
XM_011512927.1:c.795A>G	XP_011511229.1:p.Pro265=
XR_924147.1:n.884A>G
XR_924148.1:n.884A>G
XR_924149.1:n.884A>G
NM_001354579.1:c.795A>G	NP_001341508.1:p.Pro265=
XR_001740179.2:n.884A>G
XR_001740180.2:n.884A>G
XR_001740181.2:n.884A>G
XR_001740182.1:n.884A>G
XR_002959543.1:n.884A>G
XR_924148.2:n.884A>G
NM_001184.4:c.795A>G MANE Select	NP_001175.2:p.Pro265=
NM_001354579.2:c.795A>G	NP_001341508.1:p.Pro265=