Canonical Allele Identifier: CA354804134

Gene: ATR

Linked Data

• dbSNP Id: rs761413740
• MyVariant Identifiers: chr3:g.142188190C>G (hg19) ; chr3:g.142469348C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469348C>G , CM000665.2:g.142469348C>G	GRCh38
NC_000003.11:g.142188190C>G , CM000665.1:g.142188190C>G	GRCh37
NC_000003.10:g.143670880C>G	NCBI36
NG_008951.1:g.114479G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6541G>C MANE Select	ENSP00000343741.4:p.Ala2181Pro
ENST00000513291.2:n.1725G>C
ENST00000654170.1:n.1384G>C
ENST00000656590.1:c.5331G>C
ENST00000661310.1:c.6349G>C	ENSP00000499589.1:p.Ala2117Pro
ENST00000665483.1:n.396G>C
ENST00000666447.1:n.376G>C
ENST00000666943.1:n.2005G>C
ENST00000350721.8:c.6541G>C	ENSP00000343741.4:p.Ala2181Pro
ENST00000513291.1:c.80G>C
NM_001184.3:c.6541G>C	NP_001175.2:p.Ala2181Pro
XM_011512924.1:c.6547G>C	XP_011511226.1:p.Ala2183Pro
XM_011512925.1:c.6355G>C	XP_011511227.1:p.Ala2119Pro
XR_924147.1:n.6636G>C
XR_924148.1:n.6636G>C
XR_924149.1:n.6515G>C
NM_001354579.1:c.6349G>C	NP_001341508.1:p.Ala2117Pro
XR_001740179.2:n.6630G>C
XR_924148.2:n.6636G>C
NM_001184.4:c.6541G>C MANE Select	NP_001175.2:p.Ala2181Pro
NM_001354579.2:c.6349G>C	NP_001341508.1:p.Ala2117Pro