Canonical Allele Identifier: CA354804406

Gene: ATR

Linked Data

• dbSNP Id: rs1001744737
• MyVariant Identifiers: chr3:g.142188223C>G (hg19) ; chr3:g.142469381C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469381C>G , CM000665.2:g.142469381C>G	GRCh38
NC_000003.11:g.142188223C>G , CM000665.1:g.142188223C>G	GRCh37
NC_000003.10:g.143670913C>G	NCBI36
NG_008951.1:g.114446G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6508G>C MANE Select	ENSP00000343741.4:p.Ala2170Pro
ENST00000513291.2:n.1692G>C
ENST00000654170.1:n.1351G>C
ENST00000656590.1:c.5298G>C
ENST00000661310.1:c.6316G>C	ENSP00000499589.1:p.Ala2106Pro
ENST00000665483.1:n.363G>C
ENST00000666447.1:n.343G>C
ENST00000666943.1:n.1972G>C
ENST00000350721.8:c.6508G>C	ENSP00000343741.4:p.Ala2170Pro
ENST00000513291.1:c.47G>C
NM_001184.3:c.6508G>C	NP_001175.2:p.Ala2170Pro
XM_011512924.1:c.6514G>C	XP_011511226.1:p.Ala2172Pro
XM_011512925.1:c.6322G>C	XP_011511227.1:p.Ala2108Pro
XR_924147.1:n.6603G>C
XR_924148.1:n.6603G>C
XR_924149.1:n.6482G>C
NM_001354579.1:c.6316G>C	NP_001341508.1:p.Ala2106Pro
XR_001740179.2:n.6597G>C
XR_924148.2:n.6603G>C
NM_001184.4:c.6508G>C MANE Select	NP_001175.2:p.Ala2170Pro
NM_001354579.2:c.6316G>C	NP_001341508.1:p.Ala2106Pro