Canonical Allele Identifier: CA354806022

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142189005T>C (hg19) ; chr3:g.142470163T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470163T>C , CM000665.2:g.142470163T>C	GRCh38
NC_000003.11:g.142189005T>C , CM000665.1:g.142189005T>C	GRCh37
NC_000003.10:g.143671695T>C	NCBI36
NG_008951.1:g.113664A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6242A>G MANE Select	ENSP00000343741.4:p.Gln2081Arg
ENST00000513291.2:n.1426A>G
ENST00000654170.1:n.1085A>G
ENST00000656590.1:c.5032A>G
ENST00000661310.1:c.6050A>G	ENSP00000499589.1:p.Gln2017Arg
ENST00000665483.1:n.97A>G
ENST00000666447.1:n.77A>G
ENST00000666943.1:n.1706A>G
ENST00000350721.8:c.6242A>G	ENSP00000343741.4:p.Gln2081Arg
NM_001184.3:c.6242A>G	NP_001175.2:p.Gln2081Arg
XM_011512924.1:c.6248A>G	XP_011511226.1:p.Gln2083Arg
XM_011512925.1:c.6056A>G	XP_011511227.1:p.Gln2019Arg
XR_924147.1:n.6337A>G
XR_924148.1:n.6337A>G
XR_924149.1:n.6216A>G
NM_001354579.1:c.6050A>G	NP_001341508.1:p.Gln2017Arg
XR_001740179.2:n.6331A>G
XR_001740180.2:n.6385A>G
XR_001740181.2:n.6264A>G
XR_001740182.1:n.6216A>G
XR_002959543.1:n.6441A>G
XR_924148.2:n.6337A>G
NM_001184.4:c.6242A>G MANE Select	NP_001175.2:p.Gln2081Arg
NM_001354579.2:c.6050A>G	NP_001341508.1:p.Gln2017Arg