Canonical Allele Identifier: CA1406991967

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470345_142470349delinsGCTCA , CM000665.2:g.142470345_142470349delinsGCTCA	GRCh38
NC_000003.11:g.142189187_142189191delinsGCTCA , CM000665.1:g.142189187_142189191delinsGCTCA	GRCh37
NC_000003.10:g.143671877_143671881delinsGCTCA	NCBI36
NG_008951.1:g.113478_113482delinsTGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6222-166_6222-162delinsTGAGC MANE Select	ENSP00000343741.4:n.6222-166_6222-162delinsTGAGC
ENST00000513291.2:n.1406-166_1406-162delinsTGAGC
ENST00000654170.1:n.1065-166_1065-162delinsTGAGC
ENST00000656590.1:c.5012-166_5012-162delinsTGAGC
ENST00000661310.1:c.6030-166_6030-162delinsTGAGC	ENSP00000499589.1:n.6030-166_6030-162delinsTGAGC
ENST00000665483.1:n.77-166_77-162delinsTGAGC
ENST00000666447.1:n.57-166_57-162delinsTGAGC
ENST00000666943.1:n.1686-166_1686-162delinsTGAGC
ENST00000350721.8:c.6222-166_6222-162delinsTGAGC	ENSP00000343741.4:n.6222-166_6222-162delinsTGAGC
NM_001184.3:c.6222-166_6222-162delinsTGAGC	NP_001175.2:n.6222-166_6222-162delinsTGAGC
XM_011512924.1:c.6228-166_6228-162delinsTGAGC	XP_011511226.1:n.6228-166_6228-162delinsTGAGC
XM_011512925.1:c.6036-166_6036-162delinsTGAGC	XP_011511227.1:n.6036-166_6036-162delinsTGAGC
XR_924147.1:n.6317-166_6317-162delinsTGAGC
XR_924148.1:n.6317-166_6317-162delinsTGAGC
XR_924149.1:n.6196-166_6196-162delinsTGAGC
NM_001354579.1:c.6030-166_6030-162delinsTGAGC	NP_001341508.1:n.6030-166_6030-162delinsTGAGC
XR_001740179.2:n.6311-166_6311-162delinsTGAGC
XR_001740180.2:n.6365-166_6365-162delinsTGAGC
XR_001740181.2:n.6244-166_6244-162delinsTGAGC
XR_001740182.1:n.6196-166_6196-162delinsTGAGC
XR_002959543.1:n.6421-166_6421-162delinsTGAGC
XR_924148.2:n.6317-166_6317-162delinsTGAGC
NM_001184.4:c.6222-166_6222-162delinsTGAGC MANE Select	NP_001175.2:n.6222-166_6222-162delinsTGAGC
NM_001354579.2:c.6030-166_6030-162delinsTGAGC	NP_001341508.1:n.6030-166_6030-162delinsTGAGC