Canonical Allele Identifier: CA354796806

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142232377A>C (hg19) ; chr3:g.142513535A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513535A>C , CM000665.2:g.142513535A>C	GRCh38
NC_000003.11:g.142232377A>C , CM000665.1:g.142232377A>C	GRCh37
NC_000003.10:g.143715067A>C	NCBI36
NG_008951.1:g.70292T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4607T>G MANE Select	ENSP00000343741.4:p.Val1536Gly
ENST00000653868.1:n.4636T>G
ENST00000656590.1:c.3397T>G
ENST00000661310.1:c.4415T>G	ENSP00000499589.1:p.Val1472Gly
ENST00000666943.1:n.71T>G
ENST00000350721.8:c.4607T>G	ENSP00000343741.4:p.Val1536Gly
NM_001184.3:c.4607T>G	NP_001175.2:p.Val1536Gly
XM_011512924.1:c.4613T>G	XP_011511226.1:p.Val1538Gly
XM_011512925.1:c.4421T>G	XP_011511227.1:p.Val1474Gly
XM_011512926.1:c.4613T>G	XP_011511228.1:p.Val1538Gly
XM_011512927.1:c.4613T>G	XP_011511229.1:p.Val1538Gly
XR_924147.1:n.4702T>G
XR_924148.1:n.4702T>G
XR_924149.1:n.4702T>G
NM_001354579.1:c.4415T>G	NP_001341508.1:p.Val1472Gly
XR_001740179.2:n.4696T>G
XR_001740180.2:n.4702T>G
XR_001740181.2:n.4702T>G
XR_001740182.1:n.4702T>G
XR_002959543.1:n.4702T>G
XR_924148.2:n.4702T>G
NM_001184.4:c.4607T>G MANE Select	NP_001175.2:p.Val1536Gly
NM_001354579.2:c.4415T>G	NP_001341508.1:p.Val1472Gly