Canonical Allele Identifier: CA1407031597

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142562421_142562423delinsGAC , CM000665.2:g.142562421_142562423delinsGAC	GRCh38
NC_000003.11:g.142281263_142281265delinsGAC , CM000665.1:g.142281263_142281265delinsGAC	GRCh37
NC_000003.10:g.143763953_143763955delinsGAC	NCBI36
NG_008951.1:g.21404_21406delinsGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.979_981delinsGTC MANE Select	ENSP00000343741.4:p.Val327=
ENST00000515149.3:c.293-1002_293-1000delinsGTC	ENSP00000425897.3:n.293-1002_293-1000delinsGTC
ENST00000653868.1:n.1008_1010delinsGTC
ENST00000657914.1:n.3337_3339delinsGTC
ENST00000659195.1:n.3044_3046delinsGTC
ENST00000661310.1:c.979_981delinsGTC	ENSP00000499589.1:p.Val327=
ENST00000350721.8:c.979_981delinsGTC	ENSP00000343741.4:p.Val327=
ENST00000507148.1:c.293-75_293-73delinsGTC	ENSP00000426595.1:n.293-75_293-73delinsGTC
ENST00000515149.2:c.22_24delinsGTC	ENSP00000425897.2:p.Val8=
NM_001184.3:c.979_981delinsGTC	NP_001175.2:p.Val327=
XM_011512924.1:c.979_981delinsGTC	XP_011511226.1:p.Val327=
XM_011512925.1:c.979_981delinsGTC	XP_011511227.1:p.Val327=
XM_011512926.1:c.979_981delinsGTC	XP_011511228.1:p.Val327=
XM_011512927.1:c.979_981delinsGTC	XP_011511229.1:p.Val327=
XR_924147.1:n.1068_1070delinsGTC
XR_924148.1:n.1068_1070delinsGTC
XR_924149.1:n.1068_1070delinsGTC
NM_001354579.1:c.979_981delinsGTC	NP_001341508.1:p.Val327=
XR_001740179.2:n.1068_1070delinsGTC
XR_001740180.2:n.1068_1070delinsGTC
XR_001740181.2:n.1068_1070delinsGTC
XR_001740182.1:n.1068_1070delinsGTC
XR_002959543.1:n.1068_1070delinsGTC
XR_924148.2:n.1068_1070delinsGTC
NM_001184.4:c.979_981delinsGTC MANE Select	NP_001175.2:p.Val327=
NM_001354579.2:c.979_981delinsGTC	NP_001341508.1:p.Val327=