Canonical Allele Identifier: CA2668039235

Gene: ATR

Linked Data

• gnomAD v4: 3-142469972-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469972T>C , CM000665.2:g.142469972T>C	GRCh38
NC_000003.11:g.142188814T>C , CM000665.1:g.142188814T>C	GRCh37
NC_000003.10:g.143671504T>C	NCBI36
NG_008951.1:g.113855A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6319+114A>G MANE Select	ENSP00000343741.4:n.6319+114A>G
ENST00000513291.2:n.1503+114A>G
ENST00000654170.1:n.1162+114A>G
ENST00000656590.1:c.5109+114A>G
ENST00000661310.1:c.6127+114A>G	ENSP00000499589.1:n.6127+114A>G
ENST00000665483.1:n.174+114A>G
ENST00000666447.1:n.154+114A>G
ENST00000666943.1:n.1783+114A>G
ENST00000350721.8:c.6319+114A>G	ENSP00000343741.4:n.6319+114A>G
NM_001184.3:c.6319+114A>G	NP_001175.2:n.6319+114A>G
XM_011512924.1:c.6325+114A>G	XP_011511226.1:n.6325+114A>G
XM_011512925.1:c.6133+114A>G	XP_011511227.1:n.6133+114A>G
XR_924147.1:n.6414+114A>G
XR_924148.1:n.6414+114A>G
XR_924149.1:n.6293+114A>G
NM_001354579.1:c.6127+114A>G	NP_001341508.1:n.6127+114A>G
XR_001740179.2:n.6408+114A>G
XR_001740180.2:n.6462+114A>G
XR_001740181.2:n.6341+114A>G
XR_001740182.1:n.6293+114A>G
XR_002959543.1:n.6518+114A>G
XR_924148.2:n.6414+114A>G
NM_001184.4:c.6319+114A>G MANE Select	NP_001175.2:n.6319+114A>G
NM_001354579.2:c.6127+114A>G	NP_001341508.1:n.6127+114A>G