Canonical Allele Identifier: CA354805515

Gene: ATR

Linked Data

• dbSNP Id: rs2108280680
• MyVariant Identifiers: chr3:g.142188934C>T (hg19) ; chr3:g.142470092C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470092C>T , CM000665.2:g.142470092C>T	GRCh38
NC_000003.11:g.142188934C>T , CM000665.1:g.142188934C>T	GRCh37
NC_000003.10:g.143671624C>T	NCBI36
NG_008951.1:g.113735G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6313G>A MANE Select	ENSP00000343741.4:p.Glu2105Lys
ENST00000513291.2:n.1497G>A
ENST00000654170.1:n.1156G>A
ENST00000656590.1:c.5103G>A
ENST00000661310.1:c.6121G>A	ENSP00000499589.1:p.Glu2041Lys
ENST00000665483.1:n.168G>A
ENST00000666447.1:n.148G>A
ENST00000666943.1:n.1777G>A
ENST00000350721.8:c.6313G>A	ENSP00000343741.4:p.Glu2105Lys
NM_001184.3:c.6313G>A	NP_001175.2:p.Glu2105Lys
XM_011512924.1:c.6319G>A	XP_011511226.1:p.Glu2107Lys
XM_011512925.1:c.6127G>A	XP_011511227.1:p.Glu2043Lys
XR_924147.1:n.6408G>A
XR_924148.1:n.6408G>A
XR_924149.1:n.6287G>A
NM_001354579.1:c.6121G>A	NP_001341508.1:p.Glu2041Lys
XR_001740179.2:n.6402G>A
XR_001740180.2:n.6456G>A
XR_001740181.2:n.6335G>A
XR_001740182.1:n.6287G>A
XR_002959543.1:n.6512G>A
XR_924148.2:n.6408G>A
NM_001184.4:c.6313G>A MANE Select	NP_001175.2:p.Glu2105Lys
NM_001354579.2:c.6121G>A	NP_001341508.1:p.Glu2041Lys