Canonical Allele Identifier: CA2758700091

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470476C>G , CM000665.2:g.142470476C>G	GRCh38
NC_000003.11:g.142189318C>G , CM000665.1:g.142189318C>G	GRCh37
NC_000003.10:g.143672008C>G	NCBI36
NG_008951.1:g.113351G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6222-293G>C MANE Select	ENSP00000343741.4:n.6222-293G>C
ENST00000513291.2:n.1406-293G>C
ENST00000654170.1:n.1065-293G>C
ENST00000656590.1:c.5012-293G>C
ENST00000661310.1:c.6030-293G>C	ENSP00000499589.1:n.6030-293G>C
ENST00000665483.1:n.77-293G>C
ENST00000666447.1:n.57-293G>C
ENST00000666943.1:n.1686-293G>C
ENST00000350721.8:c.6222-293G>C	ENSP00000343741.4:n.6222-293G>C
NM_001184.3:c.6222-293G>C	NP_001175.2:n.6222-293G>C
XM_011512924.1:c.6228-293G>C	XP_011511226.1:n.6228-293G>C
XM_011512925.1:c.6036-293G>C	XP_011511227.1:n.6036-293G>C
XR_924147.1:n.6317-293G>C
XR_924148.1:n.6317-293G>C
XR_924149.1:n.6196-293G>C
NM_001354579.1:c.6030-293G>C	NP_001341508.1:n.6030-293G>C
XR_001740179.2:n.6311-293G>C
XR_001740180.2:n.6365-293G>C
XR_001740181.2:n.6244-293G>C
XR_001740182.1:n.6196-293G>C
XR_002959543.1:n.6421-293G>C
XR_924148.2:n.6317-293G>C
NM_001184.4:c.6222-293G>C MANE Select	NP_001175.2:n.6222-293G>C
NM_001354579.2:c.6030-293G>C	NP_001341508.1:n.6030-293G>C