Canonical Allele Identifier: CA354805706

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188970G>T (hg19) ; chr3:g.142470128G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470128G>T , CM000665.2:g.142470128G>T	GRCh38
NC_000003.11:g.142188970G>T , CM000665.1:g.142188970G>T	GRCh37
NC_000003.10:g.143671660G>T	NCBI36
NG_008951.1:g.113699C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6277C>A MANE Select	ENSP00000343741.4:p.Leu2093Ile
ENST00000513291.2:n.1461C>A
ENST00000654170.1:n.1120C>A
ENST00000656590.1:c.5067C>A
ENST00000661310.1:c.6085C>A	ENSP00000499589.1:p.Leu2029Ile
ENST00000665483.1:n.132C>A
ENST00000666447.1:n.112C>A
ENST00000666943.1:n.1741C>A
ENST00000350721.8:c.6277C>A	ENSP00000343741.4:p.Leu2093Ile
NM_001184.3:c.6277C>A	NP_001175.2:p.Leu2093Ile
XM_011512924.1:c.6283C>A	XP_011511226.1:p.Leu2095Ile
XM_011512925.1:c.6091C>A	XP_011511227.1:p.Leu2031Ile
XR_924147.1:n.6372C>A
XR_924148.1:n.6372C>A
XR_924149.1:n.6251C>A
NM_001354579.1:c.6085C>A	NP_001341508.1:p.Leu2029Ile
XR_001740179.2:n.6366C>A
XR_001740180.2:n.6420C>A
XR_001740181.2:n.6299C>A
XR_001740182.1:n.6251C>A
XR_002959543.1:n.6476C>A
XR_924148.2:n.6372C>A
NM_001184.4:c.6277C>A MANE Select	NP_001175.2:p.Leu2093Ile
NM_001354579.2:c.6085C>A	NP_001341508.1:p.Leu2029Ile