Canonical Allele Identifier: CA354806082

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142189011C>A (hg19) ; chr3:g.142470169C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470169C>A , CM000665.2:g.142470169C>A	GRCh38
NC_000003.11:g.142189011C>A , CM000665.1:g.142189011C>A	GRCh37
NC_000003.10:g.143671701C>A	NCBI36
NG_008951.1:g.113658G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6236G>T MANE Select	ENSP00000343741.4:p.Gly2079Val
ENST00000513291.2:n.1420G>T
ENST00000654170.1:n.1079G>T
ENST00000656590.1:c.5026G>T
ENST00000661310.1:c.6044G>T	ENSP00000499589.1:p.Gly2015Val
ENST00000665483.1:n.91G>T
ENST00000666447.1:n.71G>T
ENST00000666943.1:n.1700G>T
ENST00000350721.8:c.6236G>T	ENSP00000343741.4:p.Gly2079Val
NM_001184.3:c.6236G>T	NP_001175.2:p.Gly2079Val
XM_011512924.1:c.6242G>T	XP_011511226.1:p.Gly2081Val
XM_011512925.1:c.6050G>T	XP_011511227.1:p.Gly2017Val
XR_924147.1:n.6331G>T
XR_924148.1:n.6331G>T
XR_924149.1:n.6210G>T
NM_001354579.1:c.6044G>T	NP_001341508.1:p.Gly2015Val
XR_001740179.2:n.6325G>T
XR_001740180.2:n.6379G>T
XR_001740181.2:n.6258G>T
XR_001740182.1:n.6210G>T
XR_002959543.1:n.6435G>T
XR_924148.2:n.6331G>T
NM_001184.4:c.6236G>T MANE Select	NP_001175.2:p.Gly2079Val
NM_001354579.2:c.6044G>T	NP_001341508.1:p.Gly2015Val