Canonical Allele Identifier: CA354805775

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188976A>T (hg19) ; chr3:g.142470134A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470134A>T , CM000665.2:g.142470134A>T	GRCh38
NC_000003.11:g.142188976A>T , CM000665.1:g.142188976A>T	GRCh37
NC_000003.10:g.143671666A>T	NCBI36
NG_008951.1:g.113693T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6271T>A MANE Select	ENSP00000343741.4:p.Leu2091Ile
ENST00000513291.2:n.1455T>A
ENST00000654170.1:n.1114T>A
ENST00000656590.1:c.5061T>A
ENST00000661310.1:c.6079T>A	ENSP00000499589.1:p.Leu2027Ile
ENST00000665483.1:n.126T>A
ENST00000666447.1:n.106T>A
ENST00000666943.1:n.1735T>A
ENST00000350721.8:c.6271T>A	ENSP00000343741.4:p.Leu2091Ile
NM_001184.3:c.6271T>A	NP_001175.2:p.Leu2091Ile
XM_011512924.1:c.6277T>A	XP_011511226.1:p.Leu2093Ile
XM_011512925.1:c.6085T>A	XP_011511227.1:p.Leu2029Ile
XR_924147.1:n.6366T>A
XR_924148.1:n.6366T>A
XR_924149.1:n.6245T>A
NM_001354579.1:c.6079T>A	NP_001341508.1:p.Leu2027Ile
XR_001740179.2:n.6360T>A
XR_001740180.2:n.6414T>A
XR_001740181.2:n.6293T>A
XR_001740182.1:n.6245T>A
XR_002959543.1:n.6470T>A
XR_924148.2:n.6366T>A
NM_001184.4:c.6271T>A MANE Select	NP_001175.2:p.Leu2091Ile
NM_001354579.2:c.6079T>A	NP_001341508.1:p.Leu2027Ile