Canonical Allele Identifier: CA354804366

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188218A>C (hg19) ; chr3:g.142469376A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469376A>C , CM000665.2:g.142469376A>C	GRCh38
NC_000003.11:g.142188218A>C , CM000665.1:g.142188218A>C	GRCh37
NC_000003.10:g.143670908A>C	NCBI36
NG_008951.1:g.114451T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6513T>G MANE Select	ENSP00000343741.4:p.Tyr2171Ter
ENST00000513291.2:n.1697T>G
ENST00000654170.1:n.1356T>G
ENST00000656590.1:c.5303T>G
ENST00000661310.1:c.6321T>G	ENSP00000499589.1:p.Tyr2107Ter
ENST00000665483.1:n.368T>G
ENST00000666447.1:n.348T>G
ENST00000666943.1:n.1977T>G
ENST00000350721.8:c.6513T>G	ENSP00000343741.4:p.Tyr2171Ter
ENST00000513291.1:c.52T>G
NM_001184.3:c.6513T>G	NP_001175.2:p.Tyr2171Ter
XM_011512924.1:c.6519T>G	XP_011511226.1:p.Tyr2173Ter
XM_011512925.1:c.6327T>G	XP_011511227.1:p.Tyr2109Ter
XR_924147.1:n.6608T>G
XR_924148.1:n.6608T>G
XR_924149.1:n.6487T>G
NM_001354579.1:c.6321T>G	NP_001341508.1:p.Tyr2107Ter
XR_001740179.2:n.6602T>G
XR_924148.2:n.6608T>G
NM_001184.4:c.6513T>G MANE Select	NP_001175.2:p.Tyr2171Ter
NM_001354579.2:c.6321T>G	NP_001341508.1:p.Tyr2107Ter