Canonical Allele Identifier: CA354806105

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142189015A>C (hg19) ; chr3:g.142470173A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470173A>C , CM000665.2:g.142470173A>C	GRCh38
NC_000003.11:g.142189015A>C , CM000665.1:g.142189015A>C	GRCh37
NC_000003.10:g.143671705A>C	NCBI36
NG_008951.1:g.113654T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6232T>G MANE Select	ENSP00000343741.4:p.Tyr2078Asp
ENST00000513291.2:n.1416T>G
ENST00000654170.1:n.1075T>G
ENST00000656590.1:c.5022T>G
ENST00000661310.1:c.6040T>G	ENSP00000499589.1:p.Tyr2014Asp
ENST00000665483.1:n.87T>G
ENST00000666447.1:n.67T>G
ENST00000666943.1:n.1696T>G
ENST00000350721.8:c.6232T>G	ENSP00000343741.4:p.Tyr2078Asp
NM_001184.3:c.6232T>G	NP_001175.2:p.Tyr2078Asp
XM_011512924.1:c.6238T>G	XP_011511226.1:p.Tyr2080Asp
XM_011512925.1:c.6046T>G	XP_011511227.1:p.Tyr2016Asp
XR_924147.1:n.6327T>G
XR_924148.1:n.6327T>G
XR_924149.1:n.6206T>G
NM_001354579.1:c.6040T>G	NP_001341508.1:p.Tyr2014Asp
XR_001740179.2:n.6321T>G
XR_001740180.2:n.6375T>G
XR_001740181.2:n.6254T>G
XR_001740182.1:n.6206T>G
XR_002959543.1:n.6431T>G
XR_924148.2:n.6327T>G
NM_001184.4:c.6232T>G MANE Select	NP_001175.2:p.Tyr2078Asp
NM_001354579.2:c.6040T>G	NP_001341508.1:p.Tyr2014Asp