Canonical Allele Identifier: CA1407031796

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142563019_142563020delinsCA , CM000665.2:g.142563019_142563020delinsCA	GRCh38
NC_000003.11:g.142281861_142281862delinsCA , CM000665.1:g.142281861_142281862delinsCA	GRCh37
NC_000003.10:g.143764551_143764552delinsCA	NCBI36
NG_008951.1:g.20807_20808delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.382_383delinsTG MANE Select	ENSP00000343741.4:p.Cys128=
ENST00000515149.3:c.293-1599_293-1598delinsTG	ENSP00000425897.3:n.293-1599_293-1598delinsTG
ENST00000653868.1:n.411_412delinsTG
ENST00000657914.1:n.2740_2741delinsTG
ENST00000659195.1:n.2447_2448delinsTG
ENST00000661310.1:c.382_383delinsTG	ENSP00000499589.1:p.Cys128=
ENST00000350721.8:c.382_383delinsTG	ENSP00000343741.4:p.Cys128=
ENST00000507148.1:c.293-672_293-671delinsTG	ENSP00000426595.1:n.293-672_293-671delinsTG
NM_001184.3:c.382_383delinsTG	NP_001175.2:p.Cys128=
XM_011512924.1:c.382_383delinsTG	XP_011511226.1:p.Cys128=
XM_011512925.1:c.382_383delinsTG	XP_011511227.1:p.Cys128=
XM_011512926.1:c.382_383delinsTG	XP_011511228.1:p.Cys128=
XM_011512927.1:c.382_383delinsTG	XP_011511229.1:p.Cys128=
XR_924147.1:n.471_472delinsTG
XR_924148.1:n.471_472delinsTG
XR_924149.1:n.471_472delinsTG
NM_001354579.1:c.382_383delinsTG	NP_001341508.1:p.Cys128=
XR_001740179.2:n.471_472delinsTG
XR_001740180.2:n.471_472delinsTG
XR_001740181.2:n.471_472delinsTG
XR_001740182.1:n.471_472delinsTG
XR_002959543.1:n.471_472delinsTG
XR_924148.2:n.471_472delinsTG
NM_001184.4:c.382_383delinsTG MANE Select	NP_001175.2:p.Cys128=
NM_001354579.2:c.382_383delinsTG	NP_001341508.1:p.Cys128=