Canonical Allele Identifier: CA354805998

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142189002A>G (hg19) ; chr3:g.142470160A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470160A>G , CM000665.2:g.142470160A>G	GRCh38
NC_000003.11:g.142189002A>G , CM000665.1:g.142189002A>G	GRCh37
NC_000003.10:g.143671692A>G	NCBI36
NG_008951.1:g.113667T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6245T>C MANE Select	ENSP00000343741.4:p.Phe2082Ser
ENST00000513291.2:n.1429T>C
ENST00000654170.1:n.1088T>C
ENST00000656590.1:c.5035T>C
ENST00000661310.1:c.6053T>C	ENSP00000499589.1:p.Phe2018Ser
ENST00000665483.1:n.100T>C
ENST00000666447.1:n.80T>C
ENST00000666943.1:n.1709T>C
ENST00000350721.8:c.6245T>C	ENSP00000343741.4:p.Phe2082Ser
NM_001184.3:c.6245T>C	NP_001175.2:p.Phe2082Ser
XM_011512924.1:c.6251T>C	XP_011511226.1:p.Phe2084Ser
XM_011512925.1:c.6059T>C	XP_011511227.1:p.Phe2020Ser
XR_924147.1:n.6340T>C
XR_924148.1:n.6340T>C
XR_924149.1:n.6219T>C
NM_001354579.1:c.6053T>C	NP_001341508.1:p.Phe2018Ser
XR_001740179.2:n.6334T>C
XR_001740180.2:n.6388T>C
XR_001740181.2:n.6267T>C
XR_001740182.1:n.6219T>C
XR_002959543.1:n.6444T>C
XR_924148.2:n.6340T>C
NM_001184.4:c.6245T>C MANE Select	NP_001175.2:p.Phe2082Ser
NM_001354579.2:c.6053T>C	NP_001341508.1:p.Phe2018Ser