Canonical Allele Identifier: CA354805649

Gene: ATR

Linked Data

• dbSNP Id: rs2071225246
• MyVariant Identifiers: chr3:g.142188961C>G (hg19) ; chr3:g.142470119C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470119C>G , CM000665.2:g.142470119C>G	GRCh38
NC_000003.11:g.142188961C>G , CM000665.1:g.142188961C>G	GRCh37
NC_000003.10:g.143671651C>G	NCBI36
NG_008951.1:g.113708G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6286G>C MANE Select	ENSP00000343741.4:p.Asp2096His
ENST00000513291.2:n.1470G>C
ENST00000654170.1:n.1129G>C
ENST00000656590.1:c.5076G>C
ENST00000661310.1:c.6094G>C	ENSP00000499589.1:p.Asp2032His
ENST00000665483.1:n.141G>C
ENST00000666447.1:n.121G>C
ENST00000666943.1:n.1750G>C
ENST00000350721.8:c.6286G>C	ENSP00000343741.4:p.Asp2096His
NM_001184.3:c.6286G>C	NP_001175.2:p.Asp2096His
XM_011512924.1:c.6292G>C	XP_011511226.1:p.Asp2098His
XM_011512925.1:c.6100G>C	XP_011511227.1:p.Asp2034His
XR_924147.1:n.6381G>C
XR_924148.1:n.6381G>C
XR_924149.1:n.6260G>C
NM_001354579.1:c.6094G>C	NP_001341508.1:p.Asp2032His
XR_001740179.2:n.6375G>C
XR_001740180.2:n.6429G>C
XR_001740181.2:n.6308G>C
XR_001740182.1:n.6260G>C
XR_002959543.1:n.6485G>C
XR_924148.2:n.6381G>C
NM_001184.4:c.6286G>C MANE Select	NP_001175.2:p.Asp2096His
NM_001354579.2:c.6094G>C	NP_001341508.1:p.Asp2032His