Canonical Allele Identifier: CA354805683

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188969A>C (hg19) ; chr3:g.142470127A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470127A>C , CM000665.2:g.142470127A>C	GRCh38
NC_000003.11:g.142188969A>C , CM000665.1:g.142188969A>C	GRCh37
NC_000003.10:g.143671659A>C	NCBI36
NG_008951.1:g.113700T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6278T>G MANE Select	ENSP00000343741.4:p.Leu2093Arg
ENST00000513291.2:n.1462T>G
ENST00000654170.1:n.1121T>G
ENST00000656590.1:c.5068T>G
ENST00000661310.1:c.6086T>G	ENSP00000499589.1:p.Leu2029Arg
ENST00000665483.1:n.133T>G
ENST00000666447.1:n.113T>G
ENST00000666943.1:n.1742T>G
ENST00000350721.8:c.6278T>G	ENSP00000343741.4:p.Leu2093Arg
NM_001184.3:c.6278T>G	NP_001175.2:p.Leu2093Arg
XM_011512924.1:c.6284T>G	XP_011511226.1:p.Leu2095Arg
XM_011512925.1:c.6092T>G	XP_011511227.1:p.Leu2031Arg
XR_924147.1:n.6373T>G
XR_924148.1:n.6373T>G
XR_924149.1:n.6252T>G
NM_001354579.1:c.6086T>G	NP_001341508.1:p.Leu2029Arg
XR_001740179.2:n.6367T>G
XR_001740180.2:n.6421T>G
XR_001740181.2:n.6300T>G
XR_001740182.1:n.6252T>G
XR_002959543.1:n.6477T>G
XR_924148.2:n.6373T>G
NM_001184.4:c.6278T>G MANE Select	NP_001175.2:p.Leu2093Arg
NM_001354579.2:c.6086T>G	NP_001341508.1:p.Leu2029Arg