Canonical Allele Identifier: CA2668039293

Gene: ATR

Linked Data

• ClinVar Variation Id: 2786078
• ClinVar RCV Id: RCV003666241
• gnomAD v4: 3-142470196-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470196A>G , CM000665.2:g.142470196A>G	GRCh38
NC_000003.11:g.142189038A>G , CM000665.1:g.142189038A>G	GRCh37
NC_000003.10:g.143671728A>G	NCBI36
NG_008951.1:g.113631T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6222-13T>C MANE Select	ENSP00000343741.4:n.6222-13T>C
ENST00000513291.2:n.1406-13T>C
ENST00000654170.1:n.1065-13T>C
ENST00000656590.1:c.5012-13T>C
ENST00000661310.1:c.6030-13T>C	ENSP00000499589.1:n.6030-13T>C
ENST00000665483.1:n.77-13T>C
ENST00000666447.1:n.57-13T>C
ENST00000666943.1:n.1686-13T>C
ENST00000350721.8:c.6222-13T>C	ENSP00000343741.4:n.6222-13T>C
NM_001184.3:c.6222-13T>C	NP_001175.2:n.6222-13T>C
XM_011512924.1:c.6228-13T>C	XP_011511226.1:n.6228-13T>C
XM_011512925.1:c.6036-13T>C	XP_011511227.1:n.6036-13T>C
XR_924147.1:n.6317-13T>C
XR_924148.1:n.6317-13T>C
XR_924149.1:n.6196-13T>C
NM_001354579.1:c.6030-13T>C	NP_001341508.1:n.6030-13T>C
XR_001740179.2:n.6311-13T>C
XR_001740180.2:n.6365-13T>C
XR_001740181.2:n.6244-13T>C
XR_001740182.1:n.6196-13T>C
XR_002959543.1:n.6421-13T>C
XR_924148.2:n.6317-13T>C
NM_001184.4:c.6222-13T>C MANE Select	NP_001175.2:n.6222-13T>C
NM_001354579.2:c.6030-13T>C	NP_001341508.1:n.6030-13T>C