Canonical Allele Identifier: CA2668039028

Gene: ATR

Linked Data

• gnomAD v4: 3-142469277-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469277T>C , CM000665.2:g.142469277T>C	GRCh38
NC_000003.11:g.142188119T>C , CM000665.1:g.142188119T>C	GRCh37
NC_000003.10:g.143670809T>C	NCBI36
NG_008951.1:g.114550A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6552+60A>G MANE Select	ENSP00000343741.4:n.6552+60A>G
ENST00000513291.2:n.1736+60A>G
ENST00000654170.1:n.1395+60A>G
ENST00000656590.1:c.5342+60A>G
ENST00000661310.1:c.6360+60A>G	ENSP00000499589.1:n.6360+60A>G
ENST00000665483.1:n.407+60A>G
ENST00000666447.1:n.447A>G
ENST00000666943.1:n.2076A>G
ENST00000350721.8:c.6552+60A>G	ENSP00000343741.4:n.6552+60A>G
ENST00000513291.1:c.91+60A>G
NM_001184.3:c.6552+60A>G	NP_001175.2:n.6552+60A>G
XM_011512924.1:c.6558+60A>G	XP_011511226.1:n.6558+60A>G
XM_011512925.1:c.6366+60A>G	XP_011511227.1:n.6366+60A>G
XR_924147.1:n.6647+60A>G
XR_924148.1:n.6647+60A>G
XR_924149.1:n.6526+60A>G
NM_001354579.1:c.6360+60A>G	NP_001341508.1:n.6360+60A>G
XR_001740179.2:n.6641+60A>G
XR_924148.2:n.6647+60A>G
NM_001184.4:c.6552+60A>G MANE Select	NP_001175.2:n.6552+60A>G
NM_001354579.2:c.6360+60A>G	NP_001341508.1:n.6360+60A>G