Canonical Allele Identifier: CA436125974

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188976A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470134A>G , CM000665.2:g.142470134A>G	GRCh38
NC_000003.11:g.142188976A>G , CM000665.1:g.142188976A>G	GRCh37
NC_000003.10:g.143671666A>G	NCBI36
NG_008951.1:g.113693T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6271T>C MANE Select	ENSP00000343741.4:p.Leu2091=
ENST00000513291.2:n.1455T>C
ENST00000654170.1:n.1114T>C
ENST00000656590.1:c.5061T>C
ENST00000661310.1:c.6079T>C	ENSP00000499589.1:p.Leu2027=
ENST00000665483.1:n.126T>C
ENST00000666447.1:n.106T>C
ENST00000666943.1:n.1735T>C
ENST00000350721.8:c.6271T>C	ENSP00000343741.4:p.Leu2091=
NM_001184.3:c.6271T>C	NP_001175.2:p.Leu2091=
XM_011512924.1:c.6277T>C	XP_011511226.1:p.Leu2093=
XM_011512925.1:c.6085T>C	XP_011511227.1:p.Leu2029=
XR_924147.1:n.6366T>C
XR_924148.1:n.6366T>C
XR_924149.1:n.6245T>C
NM_001354579.1:c.6079T>C	NP_001341508.1:p.Leu2027=
XR_001740179.2:n.6360T>C
XR_001740180.2:n.6414T>C
XR_001740181.2:n.6293T>C
XR_001740182.1:n.6245T>C
XR_002959543.1:n.6470T>C
XR_924148.2:n.6366T>C
NM_001184.4:c.6271T>C MANE Select	NP_001175.2:p.Leu2091=
NM_001354579.2:c.6079T>C	NP_001341508.1:p.Leu2027=