Canonical Allele Identifier: CA354806046

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142189006G>C (hg19) ; chr3:g.142470164G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470164G>C , CM000665.2:g.142470164G>C	GRCh38
NC_000003.11:g.142189006G>C , CM000665.1:g.142189006G>C	GRCh37
NC_000003.10:g.143671696G>C	NCBI36
NG_008951.1:g.113663C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6241C>G MANE Select	ENSP00000343741.4:p.Gln2081Glu
ENST00000513291.2:n.1425C>G
ENST00000654170.1:n.1084C>G
ENST00000656590.1:c.5031C>G
ENST00000661310.1:c.6049C>G	ENSP00000499589.1:p.Gln2017Glu
ENST00000665483.1:n.96C>G
ENST00000666447.1:n.76C>G
ENST00000666943.1:n.1705C>G
ENST00000350721.8:c.6241C>G	ENSP00000343741.4:p.Gln2081Glu
NM_001184.3:c.6241C>G	NP_001175.2:p.Gln2081Glu
XM_011512924.1:c.6247C>G	XP_011511226.1:p.Gln2083Glu
XM_011512925.1:c.6055C>G	XP_011511227.1:p.Gln2019Glu
XR_924147.1:n.6336C>G
XR_924148.1:n.6336C>G
XR_924149.1:n.6215C>G
NM_001354579.1:c.6049C>G	NP_001341508.1:p.Gln2017Glu
XR_001740179.2:n.6330C>G
XR_001740180.2:n.6384C>G
XR_001740181.2:n.6263C>G
XR_001740182.1:n.6215C>G
XR_002959543.1:n.6440C>G
XR_924148.2:n.6336C>G
NM_001184.4:c.6241C>G MANE Select	NP_001175.2:p.Gln2081Glu
NM_001354579.2:c.6049C>G	NP_001341508.1:p.Gln2017Glu