Canonical Allele Identifier: CA354805634

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188958A>C (hg19) ; chr3:g.142470116A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470116A>C , CM000665.2:g.142470116A>C	GRCh38
NC_000003.11:g.142188958A>C , CM000665.1:g.142188958A>C	GRCh37
NC_000003.10:g.143671648A>C	NCBI36
NG_008951.1:g.113711T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6289T>G MANE Select	ENSP00000343741.4:p.Tyr2097Asp
ENST00000513291.2:n.1473T>G
ENST00000654170.1:n.1132T>G
ENST00000656590.1:c.5079T>G
ENST00000661310.1:c.6097T>G	ENSP00000499589.1:p.Tyr2033Asp
ENST00000665483.1:n.144T>G
ENST00000666447.1:n.124T>G
ENST00000666943.1:n.1753T>G
ENST00000350721.8:c.6289T>G	ENSP00000343741.4:p.Tyr2097Asp
NM_001184.3:c.6289T>G	NP_001175.2:p.Tyr2097Asp
XM_011512924.1:c.6295T>G	XP_011511226.1:p.Tyr2099Asp
XM_011512925.1:c.6103T>G	XP_011511227.1:p.Tyr2035Asp
XR_924147.1:n.6384T>G
XR_924148.1:n.6384T>G
XR_924149.1:n.6263T>G
NM_001354579.1:c.6097T>G	NP_001341508.1:p.Tyr2033Asp
XR_001740179.2:n.6378T>G
XR_001740180.2:n.6432T>G
XR_001740181.2:n.6311T>G
XR_001740182.1:n.6263T>G
XR_002959543.1:n.6488T>G
XR_924148.2:n.6384T>G
NM_001184.4:c.6289T>G MANE Select	NP_001175.2:p.Tyr2097Asp
NM_001354579.2:c.6097T>G	NP_001341508.1:p.Tyr2033Asp