Canonical Allele Identifier: CA436125953
Gene: ATR HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.142188944T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470102T>C , CM000665.2:g.142470102T>C GRCh38
NC_000003.11:g.142188944T>C , CM000665.1:g.142188944T>C GRCh37
NC_000003.10:g.143671634T>C NCBI36
NG_008951.1:g.113725A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6303A>G MANE Select ENSP00000343741.4:p.Ala2101=
ENST00000513291.2:n.1487A>G
ENST00000654170.1:n.1146A>G
ENST00000656590.1:c.5093A>G
ENST00000661310.1:c.6111A>G ENSP00000499589.1:p.Ala2037=
ENST00000665483.1:n.158A>G
ENST00000666447.1:n.138A>G
ENST00000666943.1:n.1767A>G
ENST00000350721.8:c.6303A>G ENSP00000343741.4:p.Ala2101=
NM_001184.3:c.6303A>G NP_001175.2:p.Ala2101=
XM_011512924.1:c.6309A>G XP_011511226.1:p.Ala2103=
XM_011512925.1:c.6117A>G XP_011511227.1:p.Ala2039=
XR_924147.1:n.6398A>G
XR_924148.1:n.6398A>G
XR_924149.1:n.6277A>G
NM_001354579.1:c.6111A>G NP_001341508.1:p.Ala2037=
XR_001740179.2:n.6392A>G
XR_001740180.2:n.6446A>G
XR_001740181.2:n.6325A>G
XR_001740182.1:n.6277A>G
XR_002959543.1:n.6502A>G
XR_924148.2:n.6398A>G
NM_001184.4:c.6303A>G MANE Select NP_001175.2:p.Ala2101=
NM_001354579.2:c.6111A>G NP_001341508.1:p.Ala2037=