Canonical Allele Identifier: CA84733824

Gene: ATR

Linked Data

• dbSNP Id: rs988446074
• MyVariant Identifiers: chr3:g.142189006G>A (hg19) ; chr3:g.142470164G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470164G>A , CM000665.2:g.142470164G>A	GRCh38
NC_000003.11:g.142189006G>A , CM000665.1:g.142189006G>A	GRCh37
NC_000003.10:g.143671696G>A	NCBI36
NG_008951.1:g.113663C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6241C>T MANE Select	ENSP00000343741.4:p.Gln2081Ter
ENST00000513291.2:n.1425C>T
ENST00000654170.1:n.1084C>T
ENST00000656590.1:c.5031C>T
ENST00000661310.1:c.6049C>T	ENSP00000499589.1:p.Gln2017Ter
ENST00000665483.1:n.96C>T
ENST00000666447.1:n.76C>T
ENST00000666943.1:n.1705C>T
ENST00000350721.8:c.6241C>T	ENSP00000343741.4:p.Gln2081Ter
NM_001184.3:c.6241C>T	NP_001175.2:p.Gln2081Ter
XM_011512924.1:c.6247C>T	XP_011511226.1:p.Gln2083Ter
XM_011512925.1:c.6055C>T	XP_011511227.1:p.Gln2019Ter
XR_924147.1:n.6336C>T
XR_924148.1:n.6336C>T
XR_924149.1:n.6215C>T
NM_001354579.1:c.6049C>T	NP_001341508.1:p.Gln2017Ter
XR_001740179.2:n.6330C>T
XR_001740180.2:n.6384C>T
XR_001740181.2:n.6263C>T
XR_001740182.1:n.6215C>T
XR_002959543.1:n.6440C>T
XR_924148.2:n.6336C>T
NM_001184.4:c.6241C>T MANE Select	NP_001175.2:p.Gln2081Ter
NM_001354579.2:c.6049C>T	NP_001341508.1:p.Gln2017Ter