Canonical Allele Identifier: CA354805489

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188928C>T (hg19) ; chr3:g.142470086C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470086C>T , CM000665.2:g.142470086C>T	GRCh38
NC_000003.11:g.142188928C>T , CM000665.1:g.142188928C>T	GRCh37
NC_000003.10:g.143671618C>T	NCBI36
NG_008951.1:g.113741G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6319G>A MANE Select	ENSP00000343741.4:p.Ala2107Thr
ENST00000513291.2:n.1503G>A
ENST00000654170.1:n.1162G>A
ENST00000656590.1:c.5109G>A
ENST00000661310.1:c.6127G>A	ENSP00000499589.1:p.Ala2043Thr
ENST00000665483.1:n.174G>A
ENST00000666447.1:n.154G>A
ENST00000666943.1:n.1783G>A
ENST00000350721.8:c.6319G>A	ENSP00000343741.4:p.Ala2107Thr
NM_001184.3:c.6319G>A	NP_001175.2:p.Ala2107Thr
XM_011512924.1:c.6325G>A	XP_011511226.1:p.Ala2109Thr
XM_011512925.1:c.6133G>A	XP_011511227.1:p.Ala2045Thr
XR_924147.1:n.6414G>A
XR_924148.1:n.6414G>A
XR_924149.1:n.6293G>A
NM_001354579.1:c.6127G>A	NP_001341508.1:p.Ala2043Thr
XR_001740179.2:n.6408G>A
XR_001740180.2:n.6462G>A
XR_001740181.2:n.6341G>A
XR_001740182.1:n.6293G>A
XR_002959543.1:n.6518G>A
XR_924148.2:n.6414G>A
NM_001184.4:c.6319G>A MANE Select	NP_001175.2:p.Ala2107Thr
NM_001354579.2:c.6127G>A	NP_001341508.1:p.Ala2043Thr