Canonical Allele Identifier: CA354805616

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188956A>C (hg19) ; chr3:g.142470114A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470114A>C , CM000665.2:g.142470114A>C	GRCh38
NC_000003.11:g.142188956A>C , CM000665.1:g.142188956A>C	GRCh37
NC_000003.10:g.143671646A>C	NCBI36
NG_008951.1:g.113713T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6291T>G MANE Select	ENSP00000343741.4:p.Tyr2097Ter
ENST00000513291.2:n.1475T>G
ENST00000654170.1:n.1134T>G
ENST00000656590.1:c.5081T>G
ENST00000661310.1:c.6099T>G	ENSP00000499589.1:p.Tyr2033Ter
ENST00000665483.1:n.146T>G
ENST00000666447.1:n.126T>G
ENST00000666943.1:n.1755T>G
ENST00000350721.8:c.6291T>G	ENSP00000343741.4:p.Tyr2097Ter
NM_001184.3:c.6291T>G	NP_001175.2:p.Tyr2097Ter
XM_011512924.1:c.6297T>G	XP_011511226.1:p.Tyr2099Ter
XM_011512925.1:c.6105T>G	XP_011511227.1:p.Tyr2035Ter
XR_924147.1:n.6386T>G
XR_924148.1:n.6386T>G
XR_924149.1:n.6265T>G
NM_001354579.1:c.6099T>G	NP_001341508.1:p.Tyr2033Ter
XR_001740179.2:n.6380T>G
XR_001740180.2:n.6434T>G
XR_001740181.2:n.6313T>G
XR_001740182.1:n.6265T>G
XR_002959543.1:n.6490T>G
XR_924148.2:n.6386T>G
NM_001184.4:c.6291T>G MANE Select	NP_001175.2:p.Tyr2097Ter
NM_001354579.2:c.6099T>G	NP_001341508.1:p.Tyr2033Ter