Canonical Allele Identifier: CA1406991583

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469358C= , CM000665.2:g.142469358C=	GRCh38
NC_000003.11:g.142188200C= , CM000665.1:g.142188200C=	GRCh37
NC_000003.10:g.143670890C=	NCBI36
NG_008951.1:g.114469G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6531G= MANE Select	ENSP00000343741.4:p.Trp2177=
ENST00000513291.2:n.1715G=
ENST00000654170.1:n.1374G=
ENST00000656590.1:c.5321G=
ENST00000661310.1:c.6339G=	ENSP00000499589.1:p.Trp2113=
ENST00000665483.1:n.386G=
ENST00000666447.1:n.366G=
ENST00000666943.1:n.1995G=
ENST00000350721.8:c.6531G=	ENSP00000343741.4:p.Trp2177=
ENST00000513291.1:c.70G=
NM_001184.3:c.6531G=	NP_001175.2:p.Trp2177=
XM_011512924.1:c.6537G=	XP_011511226.1:p.Trp2179=
XM_011512925.1:c.6345G=	XP_011511227.1:p.Trp2115=
XR_924147.1:n.6626G=
XR_924148.1:n.6626G=
XR_924149.1:n.6505G=
NM_001354579.1:c.6339G=	NP_001341508.1:p.Trp2113=
XR_001740179.2:n.6620G=
XR_924148.2:n.6626G=
NM_001184.4:c.6531G= MANE Select	NP_001175.2:p.Trp2177=
NM_001354579.2:c.6339G=	NP_001341508.1:p.Trp2113=