Canonical Allele Identifier: CA354796724

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142232355T>G (hg19) ; chr3:g.142513513T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513513T>G , CM000665.2:g.142513513T>G	GRCh38
NC_000003.11:g.142232355T>G , CM000665.1:g.142232355T>G	GRCh37
NC_000003.10:g.143715045T>G	NCBI36
NG_008951.1:g.70314A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.4629A>C MANE Select	ENSP00000343741.4:p.Glu1543Asp
ENST00000653868.1:n.4658A>C
ENST00000656590.1:c.3419A>C
ENST00000661310.1:c.4437A>C	ENSP00000499589.1:p.Glu1479Asp
ENST00000666943.1:n.93A>C
ENST00000350721.8:c.4629A>C	ENSP00000343741.4:p.Glu1543Asp
NM_001184.3:c.4629A>C	NP_001175.2:p.Glu1543Asp
XM_011512924.1:c.4635A>C	XP_011511226.1:p.Glu1545Asp
XM_011512925.1:c.4443A>C	XP_011511227.1:p.Glu1481Asp
XM_011512926.1:c.4635A>C	XP_011511228.1:p.Glu1545Asp
XM_011512927.1:c.4635A>C	XP_011511229.1:p.Glu1545Asp
XR_924147.1:n.4724A>C
XR_924148.1:n.4724A>C
XR_924149.1:n.4724A>C
NM_001354579.1:c.4437A>C	NP_001341508.1:p.Glu1479Asp
XR_001740179.2:n.4718A>C
XR_001740180.2:n.4724A>C
XR_001740181.2:n.4724A>C
XR_001740182.1:n.4724A>C
XR_002959543.1:n.4724A>C
XR_924148.2:n.4724A>C
NM_001184.4:c.4629A>C MANE Select	NP_001175.2:p.Glu1543Asp
NM_001354579.2:c.4437A>C	NP_001341508.1:p.Glu1479Asp