Canonical Allele Identifier: CA1406991590

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469374G= , CM000665.2:g.142469374G=	GRCh38
NC_000003.11:g.142188216G= , CM000665.1:g.142188216G=	GRCh37
NC_000003.10:g.143670906G=	NCBI36
NG_008951.1:g.114453C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6515C= MANE Select	ENSP00000343741.4:p.Pro2172=
ENST00000513291.2:n.1699C=
ENST00000654170.1:n.1358C=
ENST00000656590.1:c.5305C=
ENST00000661310.1:c.6323C=	ENSP00000499589.1:p.Pro2108=
ENST00000665483.1:n.370C=
ENST00000666447.1:n.350C=
ENST00000666943.1:n.1979C=
ENST00000350721.8:c.6515C=	ENSP00000343741.4:p.Pro2172=
ENST00000513291.1:c.54C=
NM_001184.3:c.6515C=	NP_001175.2:p.Pro2172=
XM_011512924.1:c.6521C=	XP_011511226.1:p.Pro2174=
XM_011512925.1:c.6329C=	XP_011511227.1:p.Pro2110=
XR_924147.1:n.6610C=
XR_924148.1:n.6610C=
XR_924149.1:n.6489C=
NM_001354579.1:c.6323C=	NP_001341508.1:p.Pro2108=
XR_001740179.2:n.6604C=
XR_924148.2:n.6610C=
NM_001184.4:c.6515C= MANE Select	NP_001175.2:p.Pro2172=
NM_001354579.2:c.6323C=	NP_001341508.1:p.Pro2108=