Canonical Allele Identifier: CA354804163

Gene: ATR

Linked Data

• dbSNP Id: rs2108278574
• MyVariant Identifiers: chr3:g.142188195A>T (hg19) ; chr3:g.142469353A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469353A>T , CM000665.2:g.142469353A>T	GRCh38
NC_000003.11:g.142188195A>T , CM000665.1:g.142188195A>T	GRCh37
NC_000003.10:g.143670885A>T	NCBI36
NG_008951.1:g.114474T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6536T>A MANE Select	ENSP00000343741.4:p.Met2179Lys
ENST00000513291.2:n.1720T>A
ENST00000654170.1:n.1379T>A
ENST00000656590.1:c.5326T>A
ENST00000661310.1:c.6344T>A	ENSP00000499589.1:p.Met2115Lys
ENST00000665483.1:n.391T>A
ENST00000666447.1:n.371T>A
ENST00000666943.1:n.2000T>A
ENST00000350721.8:c.6536T>A	ENSP00000343741.4:p.Met2179Lys
ENST00000513291.1:c.75T>A
NM_001184.3:c.6536T>A	NP_001175.2:p.Met2179Lys
XM_011512924.1:c.6542T>A	XP_011511226.1:p.Met2181Lys
XM_011512925.1:c.6350T>A	XP_011511227.1:p.Met2117Lys
XR_924147.1:n.6631T>A
XR_924148.1:n.6631T>A
XR_924149.1:n.6510T>A
NM_001354579.1:c.6344T>A	NP_001341508.1:p.Met2115Lys
XR_001740179.2:n.6625T>A
XR_924148.2:n.6631T>A
NM_001184.4:c.6536T>A MANE Select	NP_001175.2:p.Met2179Lys
NM_001354579.2:c.6344T>A	NP_001341508.1:p.Met2115Lys