Canonical Allele Identifier: CA436125592

Gene: ATR

Linked Data

• dbSNP Id: rs2108278477
• gnomAD v4: 3-142469337-C-T
• MyVariant Identifiers: chr3:g.142188179C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469337C>T , CM000665.2:g.142469337C>T	GRCh38
NC_000003.11:g.142188179C>T , CM000665.1:g.142188179C>T	GRCh37
NC_000003.10:g.143670869C>T	NCBI36
NG_008951.1:g.114490G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6552G>A MANE Select	ENSP00000343741.4:p.Lys2184=
ENST00000513291.2:n.1736G>A
ENST00000654170.1:n.1395G>A
ENST00000656590.1:c.5342G>A
ENST00000661310.1:c.6360G>A	ENSP00000499589.1:p.Lys2120=
ENST00000665483.1:n.407G>A
ENST00000666447.1:n.387G>A
ENST00000666943.1:n.2016G>A
ENST00000350721.8:c.6552G>A	ENSP00000343741.4:p.Lys2184=
ENST00000513291.1:c.91G>A
NM_001184.3:c.6552G>A	NP_001175.2:p.Lys2184=
XM_011512924.1:c.6558G>A	XP_011511226.1:p.Lys2186=
XM_011512925.1:c.6366G>A	XP_011511227.1:p.Lys2122=
XR_924147.1:n.6647G>A
XR_924148.1:n.6647G>A
XR_924149.1:n.6526G>A
NM_001354579.1:c.6360G>A	NP_001341508.1:p.Lys2120=
XR_001740179.2:n.6641G>A
XR_924148.2:n.6647G>A
NM_001184.4:c.6552G>A MANE Select	NP_001175.2:p.Lys2184=
NM_001354579.2:c.6360G>A	NP_001341508.1:p.Lys2120=