Canonical Allele Identifier: CA354796707

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142232351G>A (hg19) ; chr3:g.142513509G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513509G>A , CM000665.2:g.142513509G>A	GRCh38
NC_000003.11:g.142232351G>A , CM000665.1:g.142232351G>A	GRCh37
NC_000003.10:g.143715041G>A	NCBI36
NG_008951.1:g.70318C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.4633C>T MANE Select	ENSP00000343741.4:p.Gln1545Ter
ENST00000653868.1:n.4662C>T
ENST00000656590.1:c.3423C>T
ENST00000661310.1:c.4441C>T	ENSP00000499589.1:p.Gln1481Ter
ENST00000666943.1:n.97C>T
ENST00000350721.8:c.4633C>T	ENSP00000343741.4:p.Gln1545Ter
NM_001184.3:c.4633C>T	NP_001175.2:p.Gln1545Ter
XM_011512924.1:c.4639C>T	XP_011511226.1:p.Gln1547Ter
XM_011512925.1:c.4447C>T	XP_011511227.1:p.Gln1483Ter
XM_011512926.1:c.4639C>T	XP_011511228.1:p.Gln1547Ter
XM_011512927.1:c.4639C>T	XP_011511229.1:p.Gln1547Ter
XR_924147.1:n.4728C>T
XR_924148.1:n.4728C>T
XR_924149.1:n.4728C>T
NM_001354579.1:c.4441C>T	NP_001341508.1:p.Gln1481Ter
XR_001740179.2:n.4722C>T
XR_001740180.2:n.4728C>T
XR_001740181.2:n.4728C>T
XR_001740182.1:n.4728C>T
XR_002959543.1:n.4728C>T
XR_924148.2:n.4728C>T
NM_001184.4:c.4633C>T MANE Select	NP_001175.2:p.Gln1545Ter
NM_001354579.2:c.4441C>T	NP_001341508.1:p.Gln1481Ter