Canonical Allele Identifier: CA354805662

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188964G>C (hg19) ; chr3:g.142470122G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470122G>C , CM000665.2:g.142470122G>C	GRCh38
NC_000003.11:g.142188964G>C , CM000665.1:g.142188964G>C	GRCh37
NC_000003.10:g.143671654G>C	NCBI36
NG_008951.1:g.113705C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6283C>G MANE Select	ENSP00000343741.4:p.Leu2095Val
ENST00000513291.2:n.1467C>G
ENST00000654170.1:n.1126C>G
ENST00000656590.1:c.5073C>G
ENST00000661310.1:c.6091C>G	ENSP00000499589.1:p.Leu2031Val
ENST00000665483.1:n.138C>G
ENST00000666447.1:n.118C>G
ENST00000666943.1:n.1747C>G
ENST00000350721.8:c.6283C>G	ENSP00000343741.4:p.Leu2095Val
NM_001184.3:c.6283C>G	NP_001175.2:p.Leu2095Val
XM_011512924.1:c.6289C>G	XP_011511226.1:p.Leu2097Val
XM_011512925.1:c.6097C>G	XP_011511227.1:p.Leu2033Val
XR_924147.1:n.6378C>G
XR_924148.1:n.6378C>G
XR_924149.1:n.6257C>G
NM_001354579.1:c.6091C>G	NP_001341508.1:p.Leu2031Val
XR_001740179.2:n.6372C>G
XR_001740180.2:n.6426C>G
XR_001740181.2:n.6305C>G
XR_001740182.1:n.6257C>G
XR_002959543.1:n.6482C>G
XR_924148.2:n.6378C>G
NM_001184.4:c.6283C>G MANE Select	NP_001175.2:p.Leu2095Val
NM_001354579.2:c.6091C>G	NP_001341508.1:p.Leu2031Val