Canonical Allele Identifier: CA1406991573

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469326G= , CM000665.2:g.142469326G=	GRCh38
NC_000003.11:g.142188168G= , CM000665.1:g.142188168G=	GRCh37
NC_000003.10:g.143670858G=	NCBI36
NG_008951.1:g.114501C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6552+11C= MANE Select	ENSP00000343741.4:n.6552+11C=
ENST00000513291.2:n.1736+11C=
ENST00000654170.1:n.1395+11C=
ENST00000656590.1:c.5342+11C=
ENST00000661310.1:c.6360+11C=	ENSP00000499589.1:n.6360+11C=
ENST00000665483.1:n.407+11C=
ENST00000666447.1:n.398C=
ENST00000666943.1:n.2027C=
ENST00000350721.8:c.6552+11C=	ENSP00000343741.4:n.6552+11C=
ENST00000513291.1:c.91+11C=
NM_001184.3:c.6552+11C=	NP_001175.2:n.6552+11C=
XM_011512924.1:c.6558+11C=	XP_011511226.1:n.6558+11C=
XM_011512925.1:c.6366+11C=	XP_011511227.1:n.6366+11C=
XR_924147.1:n.6647+11C=
XR_924148.1:n.6647+11C=
XR_924149.1:n.6526+11C=
NM_001354579.1:c.6360+11C=	NP_001341508.1:n.6360+11C=
XR_001740179.2:n.6641+11C=
XR_924148.2:n.6647+11C=
NM_001184.4:c.6552+11C= MANE Select	NP_001175.2:n.6552+11C=
NM_001354579.2:c.6360+11C=	NP_001341508.1:n.6360+11C=