Canonical Allele Identifier: CA354796684

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142232346C>G (hg19) ; chr3:g.142513504C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513504C>G , CM000665.2:g.142513504C>G	GRCh38
NC_000003.11:g.142232346C>G , CM000665.1:g.142232346C>G	GRCh37
NC_000003.10:g.143715036C>G	NCBI36
NG_008951.1:g.70323G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.4638G>C MANE Select	ENSP00000343741.4:p.Gln1546His
ENST00000653868.1:n.4667G>C
ENST00000656590.1:c.3428G>C
ENST00000661310.1:c.4446G>C	ENSP00000499589.1:p.Gln1482His
ENST00000666943.1:n.102G>C
ENST00000350721.8:c.4638G>C	ENSP00000343741.4:p.Gln1546His
NM_001184.3:c.4638G>C	NP_001175.2:p.Gln1546His
XM_011512924.1:c.4644G>C	XP_011511226.1:p.Gln1548His
XM_011512925.1:c.4452G>C	XP_011511227.1:p.Gln1484His
XM_011512926.1:c.4644G>C	XP_011511228.1:p.Gln1548His
XM_011512927.1:c.4644G>C	XP_011511229.1:p.Gln1548His
XR_924147.1:n.4733G>C
XR_924148.1:n.4733G>C
XR_924149.1:n.4733G>C
NM_001354579.1:c.4446G>C	NP_001341508.1:p.Gln1482His
XR_001740179.2:n.4727G>C
XR_001740180.2:n.4733G>C
XR_001740181.2:n.4733G>C
XR_001740182.1:n.4733G>C
XR_002959543.1:n.4733G>C
XR_924148.2:n.4733G>C
NM_001184.4:c.4638G>C MANE Select	NP_001175.2:p.Gln1546His
NM_001354579.2:c.4446G>C	NP_001341508.1:p.Gln1482His