Canonical Allele Identifier: CA354805764

Gene: ATR

Linked Data

• COSMIC: COSM5731136
• MyVariant Identifiers: chr3:g.142188975A>G (hg19) ; chr3:g.142470133A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470133A>G , CM000665.2:g.142470133A>G	GRCh38
NC_000003.11:g.142188975A>G , CM000665.1:g.142188975A>G	GRCh37
NC_000003.10:g.143671665A>G	NCBI36
NG_008951.1:g.113694T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6272T>C MANE Select	ENSP00000343741.4:p.Leu2091Ser
ENST00000513291.2:n.1456T>C
ENST00000654170.1:n.1115T>C
ENST00000656590.1:c.5062T>C
ENST00000661310.1:c.6080T>C	ENSP00000499589.1:p.Leu2027Ser
ENST00000665483.1:n.127T>C
ENST00000666447.1:n.107T>C
ENST00000666943.1:n.1736T>C
ENST00000350721.8:c.6272T>C	ENSP00000343741.4:p.Leu2091Ser
NM_001184.3:c.6272T>C	NP_001175.2:p.Leu2091Ser
XM_011512924.1:c.6278T>C	XP_011511226.1:p.Leu2093Ser
XM_011512925.1:c.6086T>C	XP_011511227.1:p.Leu2029Ser
XR_924147.1:n.6367T>C
XR_924148.1:n.6367T>C
XR_924149.1:n.6246T>C
NM_001354579.1:c.6080T>C	NP_001341508.1:p.Leu2027Ser
XR_001740179.2:n.6361T>C
XR_001740180.2:n.6415T>C
XR_001740181.2:n.6294T>C
XR_001740182.1:n.6246T>C
XR_002959543.1:n.6471T>C
XR_924148.2:n.6367T>C
NM_001184.4:c.6272T>C MANE Select	NP_001175.2:p.Leu2091Ser
NM_001354579.2:c.6080T>C	NP_001341508.1:p.Leu2027Ser