Canonical Allele Identifier: CA354796886

Gene: ATR

Linked Data

• dbSNP Id: rs2108375337
• MyVariant Identifiers: chr3:g.142232399G>A (hg19) ; chr3:g.142513557G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513557G>A , CM000665.2:g.142513557G>A	GRCh38
NC_000003.11:g.142232399G>A , CM000665.1:g.142232399G>A	GRCh37
NC_000003.10:g.143715089G>A	NCBI36
NG_008951.1:g.70270C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4585C>T MANE Select	ENSP00000343741.4:p.Leu1529Phe
ENST00000653868.1:n.4614C>T
ENST00000656590.1:c.3375C>T
ENST00000661310.1:c.4393C>T	ENSP00000499589.1:p.Leu1465Phe
ENST00000666943.1:n.49C>T
ENST00000350721.8:c.4585C>T	ENSP00000343741.4:p.Leu1529Phe
NM_001184.3:c.4585C>T	NP_001175.2:p.Leu1529Phe
XM_011512924.1:c.4591C>T	XP_011511226.1:p.Leu1531Phe
XM_011512925.1:c.4399C>T	XP_011511227.1:p.Leu1467Phe
XM_011512926.1:c.4591C>T	XP_011511228.1:p.Leu1531Phe
XM_011512927.1:c.4591C>T	XP_011511229.1:p.Leu1531Phe
XR_924147.1:n.4680C>T
XR_924148.1:n.4680C>T
XR_924149.1:n.4680C>T
NM_001354579.1:c.4393C>T	NP_001341508.1:p.Leu1465Phe
XR_001740179.2:n.4674C>T
XR_001740180.2:n.4680C>T
XR_001740181.2:n.4680C>T
XR_001740182.1:n.4680C>T
XR_002959543.1:n.4680C>T
XR_924148.2:n.4680C>T
NM_001184.4:c.4585C>T MANE Select	NP_001175.2:p.Leu1529Phe
NM_001354579.2:c.4393C>T	NP_001341508.1:p.Leu1465Phe