Canonical Allele Identifier: CA354806135

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142189020A>G (hg19) ; chr3:g.142470178A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470178A>G , CM000665.2:g.142470178A>G	GRCh38
NC_000003.11:g.142189020A>G , CM000665.1:g.142189020A>G	GRCh37
NC_000003.10:g.143671710A>G	NCBI36
NG_008951.1:g.113649T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6227T>C MANE Select	ENSP00000343741.4:p.Leu2076Pro
ENST00000513291.2:n.1411T>C
ENST00000654170.1:n.1070T>C
ENST00000656590.1:c.5017T>C
ENST00000661310.1:c.6035T>C	ENSP00000499589.1:p.Leu2012Pro
ENST00000665483.1:n.82T>C
ENST00000666447.1:n.62T>C
ENST00000666943.1:n.1691T>C
ENST00000350721.8:c.6227T>C	ENSP00000343741.4:p.Leu2076Pro
NM_001184.3:c.6227T>C	NP_001175.2:p.Leu2076Pro
XM_011512924.1:c.6233T>C	XP_011511226.1:p.Leu2078Pro
XM_011512925.1:c.6041T>C	XP_011511227.1:p.Leu2014Pro
XR_924147.1:n.6322T>C
XR_924148.1:n.6322T>C
XR_924149.1:n.6201T>C
NM_001354579.1:c.6035T>C	NP_001341508.1:p.Leu2012Pro
XR_001740179.2:n.6316T>C
XR_001740180.2:n.6370T>C
XR_001740181.2:n.6249T>C
XR_001740182.1:n.6201T>C
XR_002959543.1:n.6426T>C
XR_924148.2:n.6322T>C
NM_001184.4:c.6227T>C MANE Select	NP_001175.2:p.Leu2076Pro
NM_001354579.2:c.6035T>C	NP_001341508.1:p.Leu2012Pro