Canonical Allele Identifier: CA354806068

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142189008T>G (hg19) ; chr3:g.142470166T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470166T>G , CM000665.2:g.142470166T>G	GRCh38
NC_000003.11:g.142189008T>G , CM000665.1:g.142189008T>G	GRCh37
NC_000003.10:g.143671698T>G	NCBI36
NG_008951.1:g.113661A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6239A>C MANE Select	ENSP00000343741.4:p.Asn2080Thr
ENST00000513291.2:n.1423A>C
ENST00000654170.1:n.1082A>C
ENST00000656590.1:c.5029A>C
ENST00000661310.1:c.6047A>C	ENSP00000499589.1:p.Asn2016Thr
ENST00000665483.1:n.94A>C
ENST00000666447.1:n.74A>C
ENST00000666943.1:n.1703A>C
ENST00000350721.8:c.6239A>C	ENSP00000343741.4:p.Asn2080Thr
NM_001184.3:c.6239A>C	NP_001175.2:p.Asn2080Thr
XM_011512924.1:c.6245A>C	XP_011511226.1:p.Asn2082Thr
XM_011512925.1:c.6053A>C	XP_011511227.1:p.Asn2018Thr
XR_924147.1:n.6334A>C
XR_924148.1:n.6334A>C
XR_924149.1:n.6213A>C
NM_001354579.1:c.6047A>C	NP_001341508.1:p.Asn2016Thr
XR_001740179.2:n.6328A>C
XR_001740180.2:n.6382A>C
XR_001740181.2:n.6261A>C
XR_001740182.1:n.6213A>C
XR_002959543.1:n.6438A>C
XR_924148.2:n.6334A>C
NM_001184.4:c.6239A>C MANE Select	NP_001175.2:p.Asn2080Thr
NM_001354579.2:c.6047A>C	NP_001341508.1:p.Asn2016Thr