Canonical Allele Identifier: CA354805566

Gene: ATR

Linked Data

• gnomAD v4: 3-142470103-G-T
• MyVariant Identifiers: chr3:g.142188945G>T (hg19) ; chr3:g.142470103G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470103G>T , CM000665.2:g.142470103G>T	GRCh38
NC_000003.11:g.142188945G>T , CM000665.1:g.142188945G>T	GRCh37
NC_000003.10:g.143671635G>T	NCBI36
NG_008951.1:g.113724C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6302C>A MANE Select	ENSP00000343741.4:p.Ala2101Glu
ENST00000513291.2:n.1486C>A
ENST00000654170.1:n.1145C>A
ENST00000656590.1:c.5092C>A
ENST00000661310.1:c.6110C>A	ENSP00000499589.1:p.Ala2037Glu
ENST00000665483.1:n.157C>A
ENST00000666447.1:n.137C>A
ENST00000666943.1:n.1766C>A
ENST00000350721.8:c.6302C>A	ENSP00000343741.4:p.Ala2101Glu
NM_001184.3:c.6302C>A	NP_001175.2:p.Ala2101Glu
XM_011512924.1:c.6308C>A	XP_011511226.1:p.Ala2103Glu
XM_011512925.1:c.6116C>A	XP_011511227.1:p.Ala2039Glu
XR_924147.1:n.6397C>A
XR_924148.1:n.6397C>A
XR_924149.1:n.6276C>A
NM_001354579.1:c.6110C>A	NP_001341508.1:p.Ala2037Glu
XR_001740179.2:n.6391C>A
XR_001740180.2:n.6445C>A
XR_001740181.2:n.6324C>A
XR_001740182.1:n.6276C>A
XR_002959543.1:n.6501C>A
XR_924148.2:n.6397C>A
NM_001184.4:c.6302C>A MANE Select	NP_001175.2:p.Ala2101Glu
NM_001354579.2:c.6110C>A	NP_001341508.1:p.Ala2037Glu