Canonical Allele Identifier: CA1407031605

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142562452_142562456delinsTAGAC , CM000665.2:g.142562452_142562456delinsTAGAC	GRCh38
NC_000003.11:g.142281294_142281298delinsTAGAC , CM000665.1:g.142281294_142281298delinsTAGAC	GRCh37
NC_000003.10:g.143763984_143763988delinsTAGAC	NCBI36
NG_008951.1:g.21371_21375delinsGTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.946_950delinsGTCTA MANE Select	ENSP00000343741.4:p.Val316=
ENST00000515149.3:c.293-1035_293-1031delinsGTCTA	ENSP00000425897.3:n.293-1035_293-1031delinsGTCTA
ENST00000653868.1:n.975_979delinsGTCTA
ENST00000657914.1:n.3304_3308delinsGTCTA
ENST00000659195.1:n.3011_3015delinsGTCTA
ENST00000661310.1:c.946_950delinsGTCTA	ENSP00000499589.1:p.Val316=
ENST00000350721.8:c.946_950delinsGTCTA	ENSP00000343741.4:p.Val316=
ENST00000507148.1:c.293-108_293-104delinsGTCTA	ENSP00000426595.1:n.293-108_293-104delinsGTCTA
NM_001184.3:c.946_950delinsGTCTA	NP_001175.2:p.Val316=
XM_011512924.1:c.946_950delinsGTCTA	XP_011511226.1:p.Val316=
XM_011512925.1:c.946_950delinsGTCTA	XP_011511227.1:p.Val316=
XM_011512926.1:c.946_950delinsGTCTA	XP_011511228.1:p.Val316=
XM_011512927.1:c.946_950delinsGTCTA	XP_011511229.1:p.Val316=
XR_924147.1:n.1035_1039delinsGTCTA
XR_924148.1:n.1035_1039delinsGTCTA
XR_924149.1:n.1035_1039delinsGTCTA
NM_001354579.1:c.946_950delinsGTCTA	NP_001341508.1:p.Val316=
XR_001740179.2:n.1035_1039delinsGTCTA
XR_001740180.2:n.1035_1039delinsGTCTA
XR_001740181.2:n.1035_1039delinsGTCTA
XR_001740182.1:n.1035_1039delinsGTCTA
XR_002959543.1:n.1035_1039delinsGTCTA
XR_924148.2:n.1035_1039delinsGTCTA
NM_001184.4:c.946_950delinsGTCTA MANE Select	NP_001175.2:p.Val316=
NM_001354579.2:c.946_950delinsGTCTA	NP_001341508.1:p.Val316=