Canonical Allele Identifier: CA436125623

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188206T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469364T>G , CM000665.2:g.142469364T>G	GRCh38
NC_000003.11:g.142188206T>G , CM000665.1:g.142188206T>G	GRCh37
NC_000003.10:g.143670896T>G	NCBI36
NG_008951.1:g.114463A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6525A>C MANE Select	ENSP00000343741.4:p.Ala2175=
ENST00000513291.2:n.1709A>C
ENST00000654170.1:n.1368A>C
ENST00000656590.1:c.5315A>C
ENST00000661310.1:c.6333A>C	ENSP00000499589.1:p.Ala2111=
ENST00000665483.1:n.380A>C
ENST00000666447.1:n.360A>C
ENST00000666943.1:n.1989A>C
ENST00000350721.8:c.6525A>C	ENSP00000343741.4:p.Ala2175=
ENST00000513291.1:c.64A>C
NM_001184.3:c.6525A>C	NP_001175.2:p.Ala2175=
XM_011512924.1:c.6531A>C	XP_011511226.1:p.Ala2177=
XM_011512925.1:c.6339A>C	XP_011511227.1:p.Ala2113=
XR_924147.1:n.6620A>C
XR_924148.1:n.6620A>C
XR_924149.1:n.6499A>C
NM_001354579.1:c.6333A>C	NP_001341508.1:p.Ala2111=
XR_001740179.2:n.6614A>C
XR_924148.2:n.6620A>C
NM_001184.4:c.6525A>C MANE Select	NP_001175.2:p.Ala2175=
NM_001354579.2:c.6333A>C	NP_001341508.1:p.Ala2111=