Canonical Allele Identifier: CA354804379

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188219T>C (hg19) ; chr3:g.142469377T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469377T>C , CM000665.2:g.142469377T>C	GRCh38
NC_000003.11:g.142188219T>C , CM000665.1:g.142188219T>C	GRCh37
NC_000003.10:g.143670909T>C	NCBI36
NG_008951.1:g.114450A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6512A>G MANE Select	ENSP00000343741.4:p.Tyr2171Cys
ENST00000513291.2:n.1696A>G
ENST00000654170.1:n.1355A>G
ENST00000656590.1:c.5302A>G
ENST00000661310.1:c.6320A>G	ENSP00000499589.1:p.Tyr2107Cys
ENST00000665483.1:n.367A>G
ENST00000666447.1:n.347A>G
ENST00000666943.1:n.1976A>G
ENST00000350721.8:c.6512A>G	ENSP00000343741.4:p.Tyr2171Cys
ENST00000513291.1:c.51A>G
NM_001184.3:c.6512A>G	NP_001175.2:p.Tyr2171Cys
XM_011512924.1:c.6518A>G	XP_011511226.1:p.Tyr2173Cys
XM_011512925.1:c.6326A>G	XP_011511227.1:p.Tyr2109Cys
XR_924147.1:n.6607A>G
XR_924148.1:n.6607A>G
XR_924149.1:n.6486A>G
NM_001354579.1:c.6320A>G	NP_001341508.1:p.Tyr2107Cys
XR_001740179.2:n.6601A>G
XR_924148.2:n.6607A>G
NM_001184.4:c.6512A>G MANE Select	NP_001175.2:p.Tyr2171Cys
NM_001354579.2:c.6320A>G	NP_001341508.1:p.Tyr2107Cys