Canonical Allele Identifier: CA1407031685

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142562680_142562681delinsCT , CM000665.2:g.142562680_142562681delinsCT	GRCh38
NC_000003.11:g.142281522_142281523delinsCT , CM000665.1:g.142281522_142281523delinsCT	GRCh37
NC_000003.10:g.143764212_143764213delinsCT	NCBI36
NG_008951.1:g.21146_21147delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.721_722delinsAG MANE Select	ENSP00000343741.4:p.Ser241=
ENST00000515149.3:c.293-1260_293-1259delinsAG	ENSP00000425897.3:n.293-1260_293-1259delinsAG
ENST00000653868.1:n.750_751delinsAG
ENST00000657914.1:n.3079_3080delinsAG
ENST00000659195.1:n.2786_2787delinsAG
ENST00000661310.1:c.721_722delinsAG	ENSP00000499589.1:p.Ser241=
ENST00000350721.8:c.721_722delinsAG	ENSP00000343741.4:p.Ser241=
ENST00000507148.1:c.293-333_293-332delinsAG	ENSP00000426595.1:n.293-333_293-332delinsAG
NM_001184.3:c.721_722delinsAG	NP_001175.2:p.Ser241=
XM_011512924.1:c.721_722delinsAG	XP_011511226.1:p.Ser241=
XM_011512925.1:c.721_722delinsAG	XP_011511227.1:p.Ser241=
XM_011512926.1:c.721_722delinsAG	XP_011511228.1:p.Ser241=
XM_011512927.1:c.721_722delinsAG	XP_011511229.1:p.Ser241=
XR_924147.1:n.810_811delinsAG
XR_924148.1:n.810_811delinsAG
XR_924149.1:n.810_811delinsAG
NM_001354579.1:c.721_722delinsAG	NP_001341508.1:p.Ser241=
XR_001740179.2:n.810_811delinsAG
XR_001740180.2:n.810_811delinsAG
XR_001740181.2:n.810_811delinsAG
XR_001740182.1:n.810_811delinsAG
XR_002959543.1:n.810_811delinsAG
XR_924148.2:n.810_811delinsAG
NM_001184.4:c.721_722delinsAG MANE Select	NP_001175.2:p.Ser241=
NM_001354579.2:c.721_722delinsAG	NP_001341508.1:p.Ser241=