Canonical Allele Identifier: CA436125990

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142189007A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470165A>G , CM000665.2:g.142470165A>G	GRCh38
NC_000003.11:g.142189007A>G , CM000665.1:g.142189007A>G	GRCh37
NC_000003.10:g.143671697A>G	NCBI36
NG_008951.1:g.113662T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6240T>C MANE Select	ENSP00000343741.4:p.Asn2080=
ENST00000513291.2:n.1424T>C
ENST00000654170.1:n.1083T>C
ENST00000656590.1:c.5030T>C
ENST00000661310.1:c.6048T>C	ENSP00000499589.1:p.Asn2016=
ENST00000665483.1:n.95T>C
ENST00000666447.1:n.75T>C
ENST00000666943.1:n.1704T>C
ENST00000350721.8:c.6240T>C	ENSP00000343741.4:p.Asn2080=
NM_001184.3:c.6240T>C	NP_001175.2:p.Asn2080=
XM_011512924.1:c.6246T>C	XP_011511226.1:p.Asn2082=
XM_011512925.1:c.6054T>C	XP_011511227.1:p.Asn2018=
XR_924147.1:n.6335T>C
XR_924148.1:n.6335T>C
XR_924149.1:n.6214T>C
NM_001354579.1:c.6048T>C	NP_001341508.1:p.Asn2016=
XR_001740179.2:n.6329T>C
XR_001740180.2:n.6383T>C
XR_001740181.2:n.6262T>C
XR_001740182.1:n.6214T>C
XR_002959543.1:n.6439T>C
XR_924148.2:n.6335T>C
NM_001184.4:c.6240T>C MANE Select	NP_001175.2:p.Asn2080=
NM_001354579.2:c.6048T>C	NP_001341508.1:p.Asn2016=