Canonical Allele Identifier: CA354805931

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188994G>C (hg19) ; chr3:g.142470152G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470152G>C , CM000665.2:g.142470152G>C	GRCh38
NC_000003.11:g.142188994G>C , CM000665.1:g.142188994G>C	GRCh37
NC_000003.10:g.143671684G>C	NCBI36
NG_008951.1:g.113675C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6253C>G MANE Select	ENSP00000343741.4:p.Gln2085Glu
ENST00000513291.2:n.1437C>G
ENST00000654170.1:n.1096C>G
ENST00000656590.1:c.5043C>G
ENST00000661310.1:c.6061C>G	ENSP00000499589.1:p.Gln2021Glu
ENST00000665483.1:n.108C>G
ENST00000666447.1:n.88C>G
ENST00000666943.1:n.1717C>G
ENST00000350721.8:c.6253C>G	ENSP00000343741.4:p.Gln2085Glu
NM_001184.3:c.6253C>G	NP_001175.2:p.Gln2085Glu
XM_011512924.1:c.6259C>G	XP_011511226.1:p.Gln2087Glu
XM_011512925.1:c.6067C>G	XP_011511227.1:p.Gln2023Glu
XR_924147.1:n.6348C>G
XR_924148.1:n.6348C>G
XR_924149.1:n.6227C>G
NM_001354579.1:c.6061C>G	NP_001341508.1:p.Gln2021Glu
XR_001740179.2:n.6342C>G
XR_001740180.2:n.6396C>G
XR_001740181.2:n.6275C>G
XR_001740182.1:n.6227C>G
XR_002959543.1:n.6452C>G
XR_924148.2:n.6348C>G
NM_001184.4:c.6253C>G MANE Select	NP_001175.2:p.Gln2085Glu
NM_001354579.2:c.6061C>G	NP_001341508.1:p.Gln2021Glu