Canonical Allele Identifier: CA2668039279

Gene: ATR

Linked Data

• gnomAD v4: 3-142470077-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470078del , CM000665.2:g.142470078del	GRCh38
NC_000003.11:g.142188920del , CM000665.1:g.142188920del	GRCh37
NC_000003.10:g.143671610del	NCBI36
NG_008951.1:g.113749del

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6319+8del MANE Select	ENSP00000343741.4:n.6319+8del
ENST00000513291.2:n.1503+8del
ENST00000654170.1:n.1162+8del
ENST00000656590.1:c.5109+8del
ENST00000661310.1:c.6127+8del	ENSP00000499589.1:n.6127+8del
ENST00000665483.1:n.174+8del
ENST00000666447.1:n.154+8del
ENST00000666943.1:n.1783+8del
ENST00000350721.8:c.6319+8del	ENSP00000343741.4:n.6319+8del
NM_001184.3:c.6319+8del	NP_001175.2:n.6319+8del
XM_011512924.1:c.6325+8del	XP_011511226.1:n.6325+8del
XM_011512925.1:c.6133+8del	XP_011511227.1:n.6133+8del
XR_924147.1:n.6414+8del
XR_924148.1:n.6414+8del
XR_924149.1:n.6293+8del
NM_001354579.1:c.6127+8del	NP_001341508.1:n.6127+8del
XR_001740179.2:n.6408+8del
XR_001740180.2:n.6462+8del
XR_001740181.2:n.6341+8del
XR_001740182.1:n.6293+8del
XR_002959543.1:n.6518+8del
XR_924148.2:n.6414+8del
NM_001184.4:c.6319+8del MANE Select	NP_001175.2:n.6319+8del
NM_001354579.2:c.6127+8del	NP_001341508.1:n.6127+8del