Canonical Allele Identifier: CA354804361

Gene: ATR

Linked Data

• dbSNP Id: rs2071204828
• COSMIC: COSM5429360
• MyVariant Identifiers: chr3:g.142188216G>C (hg19) ; chr3:g.142469374G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469374G>C , CM000665.2:g.142469374G>C	GRCh38
NC_000003.11:g.142188216G>C , CM000665.1:g.142188216G>C	GRCh37
NC_000003.10:g.143670906G>C	NCBI36
NG_008951.1:g.114453C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6515C>G MANE Select	ENSP00000343741.4:p.Pro2172Arg
ENST00000513291.2:n.1699C>G
ENST00000654170.1:n.1358C>G
ENST00000656590.1:c.5305C>G
ENST00000661310.1:c.6323C>G	ENSP00000499589.1:p.Pro2108Arg
ENST00000665483.1:n.370C>G
ENST00000666447.1:n.350C>G
ENST00000666943.1:n.1979C>G
ENST00000350721.8:c.6515C>G	ENSP00000343741.4:p.Pro2172Arg
ENST00000513291.1:c.54C>G
NM_001184.3:c.6515C>G	NP_001175.2:p.Pro2172Arg
XM_011512924.1:c.6521C>G	XP_011511226.1:p.Pro2174Arg
XM_011512925.1:c.6329C>G	XP_011511227.1:p.Pro2110Arg
XR_924147.1:n.6610C>G
XR_924148.1:n.6610C>G
XR_924149.1:n.6489C>G
NM_001354579.1:c.6323C>G	NP_001341508.1:p.Pro2108Arg
XR_001740179.2:n.6604C>G
XR_924148.2:n.6610C>G
NM_001184.4:c.6515C>G MANE Select	NP_001175.2:p.Pro2172Arg
NM_001354579.2:c.6323C>G	NP_001341508.1:p.Pro2108Arg