Canonical Allele Identifier: CA354805606

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188954C>T (hg19) ; chr3:g.142470112C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470112C>T , CM000665.2:g.142470112C>T	GRCh38
NC_000003.11:g.142188954C>T , CM000665.1:g.142188954C>T	GRCh37
NC_000003.10:g.143671644C>T	NCBI36
NG_008951.1:g.113715G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6293G>A MANE Select	ENSP00000343741.4:p.Gly2098Asp
ENST00000513291.2:n.1477G>A
ENST00000654170.1:n.1136G>A
ENST00000656590.1:c.5083G>A
ENST00000661310.1:c.6101G>A	ENSP00000499589.1:p.Gly2034Asp
ENST00000665483.1:n.148G>A
ENST00000666447.1:n.128G>A
ENST00000666943.1:n.1757G>A
ENST00000350721.8:c.6293G>A	ENSP00000343741.4:p.Gly2098Asp
NM_001184.3:c.6293G>A	NP_001175.2:p.Gly2098Asp
XM_011512924.1:c.6299G>A	XP_011511226.1:p.Gly2100Asp
XM_011512925.1:c.6107G>A	XP_011511227.1:p.Gly2036Asp
XR_924147.1:n.6388G>A
XR_924148.1:n.6388G>A
XR_924149.1:n.6267G>A
NM_001354579.1:c.6101G>A	NP_001341508.1:p.Gly2034Asp
XR_001740179.2:n.6382G>A
XR_001740180.2:n.6436G>A
XR_001740181.2:n.6315G>A
XR_001740182.1:n.6267G>A
XR_002959543.1:n.6492G>A
XR_924148.2:n.6388G>A
NM_001184.4:c.6293G>A MANE Select	NP_001175.2:p.Gly2098Asp
NM_001354579.2:c.6101G>A	NP_001341508.1:p.Gly2034Asp