Canonical Allele Identifier: CA354805741

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188972G>A (hg19) ; chr3:g.142470130G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470130G>A , CM000665.2:g.142470130G>A	GRCh38
NC_000003.11:g.142188972G>A , CM000665.1:g.142188972G>A	GRCh37
NC_000003.10:g.143671662G>A	NCBI36
NG_008951.1:g.113697C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6275C>T MANE Select	ENSP00000343741.4:p.Thr2092Ile
ENST00000513291.2:n.1459C>T
ENST00000654170.1:n.1118C>T
ENST00000656590.1:c.5065C>T
ENST00000661310.1:c.6083C>T	ENSP00000499589.1:p.Thr2028Ile
ENST00000665483.1:n.130C>T
ENST00000666447.1:n.110C>T
ENST00000666943.1:n.1739C>T
ENST00000350721.8:c.6275C>T	ENSP00000343741.4:p.Thr2092Ile
NM_001184.3:c.6275C>T	NP_001175.2:p.Thr2092Ile
XM_011512924.1:c.6281C>T	XP_011511226.1:p.Thr2094Ile
XM_011512925.1:c.6089C>T	XP_011511227.1:p.Thr2030Ile
XR_924147.1:n.6370C>T
XR_924148.1:n.6370C>T
XR_924149.1:n.6249C>T
NM_001354579.1:c.6083C>T	NP_001341508.1:p.Thr2028Ile
XR_001740179.2:n.6364C>T
XR_001740180.2:n.6418C>T
XR_001740181.2:n.6297C>T
XR_001740182.1:n.6249C>T
XR_002959543.1:n.6474C>T
XR_924148.2:n.6370C>T
NM_001184.4:c.6275C>T MANE Select	NP_001175.2:p.Thr2092Ile
NM_001354579.2:c.6083C>T	NP_001341508.1:p.Thr2028Ile