Canonical Allele Identifier: CA436125965

Gene: ATR

Linked Data

• gnomAD v4: 3-142470120-A-G
• MyVariant Identifiers: chr3:g.142188962A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470120A>G , CM000665.2:g.142470120A>G	GRCh38
NC_000003.11:g.142188962A>G , CM000665.1:g.142188962A>G	GRCh37
NC_000003.10:g.143671652A>G	NCBI36
NG_008951.1:g.113707T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6285T>C MANE Select	ENSP00000343741.4:p.Leu2095=
ENST00000513291.2:n.1469T>C
ENST00000654170.1:n.1128T>C
ENST00000656590.1:c.5075T>C
ENST00000661310.1:c.6093T>C	ENSP00000499589.1:p.Leu2031=
ENST00000665483.1:n.140T>C
ENST00000666447.1:n.120T>C
ENST00000666943.1:n.1749T>C
ENST00000350721.8:c.6285T>C	ENSP00000343741.4:p.Leu2095=
NM_001184.3:c.6285T>C	NP_001175.2:p.Leu2095=
XM_011512924.1:c.6291T>C	XP_011511226.1:p.Leu2097=
XM_011512925.1:c.6099T>C	XP_011511227.1:p.Leu2033=
XR_924147.1:n.6380T>C
XR_924148.1:n.6380T>C
XR_924149.1:n.6259T>C
NM_001354579.1:c.6093T>C	NP_001341508.1:p.Leu2031=
XR_001740179.2:n.6374T>C
XR_001740180.2:n.6428T>C
XR_001740181.2:n.6307T>C
XR_001740182.1:n.6259T>C
XR_002959543.1:n.6484T>C
XR_924148.2:n.6380T>C
NM_001184.4:c.6285T>C MANE Select	NP_001175.2:p.Leu2095=
NM_001354579.2:c.6093T>C	NP_001341508.1:p.Leu2031=