Canonical Allele Identifier: CA436126002

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142189022A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470180A>G , CM000665.2:g.142470180A>G	GRCh38
NC_000003.11:g.142189022A>G , CM000665.1:g.142189022A>G	GRCh37
NC_000003.10:g.143671712A>G	NCBI36
NG_008951.1:g.113647T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6225T>C MANE Select	ENSP00000343741.4:p.Ser2075=
ENST00000513291.2:n.1409T>C
ENST00000654170.1:n.1068T>C
ENST00000656590.1:c.5015T>C
ENST00000661310.1:c.6033T>C	ENSP00000499589.1:p.Ser2011=
ENST00000665483.1:n.80T>C
ENST00000666447.1:n.60T>C
ENST00000666943.1:n.1689T>C
ENST00000350721.8:c.6225T>C	ENSP00000343741.4:p.Ser2075=
NM_001184.3:c.6225T>C	NP_001175.2:p.Ser2075=
XM_011512924.1:c.6231T>C	XP_011511226.1:p.Ser2077=
XM_011512925.1:c.6039T>C	XP_011511227.1:p.Ser2013=
XR_924147.1:n.6320T>C
XR_924148.1:n.6320T>C
XR_924149.1:n.6199T>C
NM_001354579.1:c.6033T>C	NP_001341508.1:p.Ser2011=
XR_001740179.2:n.6314T>C
XR_001740180.2:n.6368T>C
XR_001740181.2:n.6247T>C
XR_001740182.1:n.6199T>C
XR_002959543.1:n.6424T>C
XR_924148.2:n.6320T>C
NM_001184.4:c.6225T>C MANE Select	NP_001175.2:p.Ser2075=
NM_001354579.2:c.6033T>C	NP_001341508.1:p.Ser2011=