Canonical Allele Identifier: CA436127725

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142485199T>C , CM000665.2:g.142485199T>C	GRCh38
NC_000003.11:g.142204041T>C , CM000665.1:g.142204041T>C	GRCh37
NC_000003.10:g.143686731T>C	NCBI36
NG_008951.1:g.98628A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001184.4:c.6162A>G MANE Select	NP_001175.2:p.Thr2054=
ENST00000350721.9:c.6162A>G MANE Select	ENSP00000343741.4:p.Thr2054=
NM_001184.3:c.6162A>G	NP_001175.2:p.Thr2054=
NM_001354579.1:c.5970A>G	NP_001341508.1:p.Thr1990=
NM_001354579.2:c.5970A>G	NP_001341508.1:p.Thr1990=
ENST00000350721.8:c.6162A>G	ENSP00000343741.4:p.Thr2054=
ENST00000513291.2:n.1346A>G
ENST00000654170.1:n.1005A>G
ENST00000656590.1:c.4952A>G
ENST00000661310.1:c.5970A>G	ENSP00000499589.1:p.Thr1990=
ENST00000665483.1:n.17A>G
ENST00000666943.1:n.1626A>G
XM_011512924.1:c.6168A>G	XP_011511226.1:p.Thr2056=
XM_011512925.1:c.5976A>G	XP_011511227.1:p.Thr1992=
XM_011512926.1:c.6168A>G	XP_011511228.1:p.Thr2056=
XR_001740179.2:n.6251A>G
XR_001740180.2:n.6305A>G
XR_001740181.2:n.6184A>G
XR_001740182.1:n.6136A>G
XR_002959543.1:n.6257A>G
XR_924147.1:n.6257A>G
XR_924148.1:n.6257A>G
XR_924148.2:n.6257A>G
XR_924149.1:n.6136A>G