Canonical Allele Identifier: CA354823381

Gene: ATR

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142561367C>G , CM000665.2:g.142561367C>G	GRCh38
NC_000003.11:g.142280209C>G , CM000665.1:g.142280209C>G	GRCh37
NC_000003.10:g.143762899C>G	NCBI36
NG_008951.1:g.22460G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.1225G>C MANE Select	ENSP00000343741.4:p.Glu409Gln
ENST00000515149.3:c.347G>C	ENSP00000425897.3:p.Ter116Ser
ENST00000653868.1:n.1254G>C
ENST00000656590.1:c.15G>C
ENST00000657914.1:n.3583G>C
ENST00000659195.1:n.4100G>C
ENST00000661310.1:c.1225G>C	ENSP00000499589.1:p.Glu409Gln
ENST00000350721.8:c.1225G>C	ENSP00000343741.4:p.Glu409Gln
ENST00000507148.1:c.*161G>C	ENSP00000426595.1:n.*161G>C
ENST00000515149.2:c.268G>C	ENSP00000425897.2:p.Glu90Gln
NM_001184.3:c.1225G>C	NP_001175.2:p.Glu409Gln
XM_011512924.1:c.1225G>C	XP_011511226.1:p.Glu409Gln
XM_011512925.1:c.1225G>C	XP_011511227.1:p.Glu409Gln
XM_011512926.1:c.1225G>C	XP_011511228.1:p.Glu409Gln
XM_011512927.1:c.1225G>C	XP_011511229.1:p.Glu409Gln
XR_924147.1:n.1314G>C
XR_924148.1:n.1314G>C
XR_924149.1:n.1314G>C
NM_001354579.1:c.1225G>C	NP_001341508.1:p.Glu409Gln
XR_001740179.2:n.1314G>C
XR_001740180.2:n.1314G>C
XR_001740181.2:n.1314G>C
XR_001740182.1:n.1314G>C
XR_002959543.1:n.1314G>C
XR_924148.2:n.1314G>C
NM_001184.4:c.1225G>C MANE Select	NP_001175.2:p.Glu409Gln
NM_001354579.2:c.1225G>C	NP_001341508.1:p.Glu409Gln