Canonical Allele Identifier: CA354804115

Gene: ATR

Linked Data

• dbSNP Id: rs2108278515
• MyVariant Identifiers: chr3:g.142188186A>T (hg19) ; chr3:g.142469344A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469344A>T , CM000665.2:g.142469344A>T	GRCh38
NC_000003.11:g.142188186A>T , CM000665.1:g.142188186A>T	GRCh37
NC_000003.10:g.143670876A>T	NCBI36
NG_008951.1:g.114483T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6545T>A MANE Select	ENSP00000343741.4:p.Val2182Glu
ENST00000513291.2:n.1729T>A
ENST00000654170.1:n.1388T>A
ENST00000656590.1:c.5335T>A
ENST00000661310.1:c.6353T>A	ENSP00000499589.1:p.Val2118Glu
ENST00000665483.1:n.400T>A
ENST00000666447.1:n.380T>A
ENST00000666943.1:n.2009T>A
ENST00000350721.8:c.6545T>A	ENSP00000343741.4:p.Val2182Glu
ENST00000513291.1:c.84T>A
NM_001184.3:c.6545T>A	NP_001175.2:p.Val2182Glu
XM_011512924.1:c.6551T>A	XP_011511226.1:p.Val2184Glu
XM_011512925.1:c.6359T>A	XP_011511227.1:p.Val2120Glu
XR_924147.1:n.6640T>A
XR_924148.1:n.6640T>A
XR_924149.1:n.6519T>A
NM_001354579.1:c.6353T>A	NP_001341508.1:p.Val2118Glu
XR_001740179.2:n.6634T>A
XR_924148.2:n.6640T>A
NM_001184.4:c.6545T>A MANE Select	NP_001175.2:p.Val2182Glu
NM_001354579.2:c.6353T>A	NP_001341508.1:p.Val2118Glu