Canonical Allele Identifier: CA354806010

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142189003A>G (hg19) ; chr3:g.142470161A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470161A>G , CM000665.2:g.142470161A>G	GRCh38
NC_000003.11:g.142189003A>G , CM000665.1:g.142189003A>G	GRCh37
NC_000003.10:g.143671693A>G	NCBI36
NG_008951.1:g.113666T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6244T>C MANE Select	ENSP00000343741.4:p.Phe2082Leu
ENST00000513291.2:n.1428T>C
ENST00000654170.1:n.1087T>C
ENST00000656590.1:c.5034T>C
ENST00000661310.1:c.6052T>C	ENSP00000499589.1:p.Phe2018Leu
ENST00000665483.1:n.99T>C
ENST00000666447.1:n.79T>C
ENST00000666943.1:n.1708T>C
ENST00000350721.8:c.6244T>C	ENSP00000343741.4:p.Phe2082Leu
NM_001184.3:c.6244T>C	NP_001175.2:p.Phe2082Leu
XM_011512924.1:c.6250T>C	XP_011511226.1:p.Phe2084Leu
XM_011512925.1:c.6058T>C	XP_011511227.1:p.Phe2020Leu
XR_924147.1:n.6339T>C
XR_924148.1:n.6339T>C
XR_924149.1:n.6218T>C
NM_001354579.1:c.6052T>C	NP_001341508.1:p.Phe2018Leu
XR_001740179.2:n.6333T>C
XR_001740180.2:n.6387T>C
XR_001740181.2:n.6266T>C
XR_001740182.1:n.6218T>C
XR_002959543.1:n.6443T>C
XR_924148.2:n.6339T>C
NM_001184.4:c.6244T>C MANE Select	NP_001175.2:p.Phe2082Leu
NM_001354579.2:c.6052T>C	NP_001341508.1:p.Phe2018Leu