Canonical Allele Identifier: CA436125969

Gene: ATR

Linked Data

• gnomAD v4: 3-142470128-G-A
• MyVariant Identifiers: chr3:g.142188970G>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6277C>T MANE Select	ENSP00000343741.4:p.Leu2093=
ENST00000513291.2:n.1461C>T
ENST00000654170.1:n.1120C>T
ENST00000656590.1:c.5067C>T
ENST00000661310.1:c.6085C>T	ENSP00000499589.1:p.Leu2029=
ENST00000665483.1:n.132C>T
ENST00000666447.1:n.112C>T
ENST00000666943.1:n.1741C>T
ENST00000350721.8:c.6277C>T	ENSP00000343741.4:p.Leu2093=
NM_001184.3:c.6277C>T	NP_001175.2:p.Leu2093=
XM_011512924.1:c.6283C>T	XP_011511226.1:p.Leu2095=
XM_011512925.1:c.6091C>T	XP_011511227.1:p.Leu2031=
XR_924147.1:n.6372C>T
XR_924148.1:n.6372C>T
XR_924149.1:n.6251C>T
NM_001354579.1:c.6085C>T	NP_001341508.1:p.Leu2029=
XR_001740179.2:n.6366C>T
XR_001740180.2:n.6420C>T
XR_001740181.2:n.6299C>T
XR_001740182.1:n.6251C>T
XR_002959543.1:n.6476C>T
XR_924148.2:n.6372C>T
NM_001184.4:c.6277C>T MANE Select	NP_001175.2:p.Leu2093=
NM_001354579.2:c.6085C>T	NP_001341508.1:p.Leu2029=