Canonical Allele Identifier: CA354804105

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188184A>C (hg19) ; chr3:g.142469342A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469342A>C , CM000665.2:g.142469342A>C	GRCh38
NC_000003.11:g.142188184A>C , CM000665.1:g.142188184A>C	GRCh37
NC_000003.10:g.143670874A>C	NCBI36
NG_008951.1:g.114485T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6547T>G MANE Select	ENSP00000343741.4:p.Ser2183Ala
ENST00000513291.2:n.1731T>G
ENST00000654170.1:n.1390T>G
ENST00000656590.1:c.5337T>G
ENST00000661310.1:c.6355T>G	ENSP00000499589.1:p.Ser2119Ala
ENST00000665483.1:n.402T>G
ENST00000666447.1:n.382T>G
ENST00000666943.1:n.2011T>G
ENST00000350721.8:c.6547T>G	ENSP00000343741.4:p.Ser2183Ala
ENST00000513291.1:c.86T>G
NM_001184.3:c.6547T>G	NP_001175.2:p.Ser2183Ala
XM_011512924.1:c.6553T>G	XP_011511226.1:p.Ser2185Ala
XM_011512925.1:c.6361T>G	XP_011511227.1:p.Ser2121Ala
XR_924147.1:n.6642T>G
XR_924148.1:n.6642T>G
XR_924149.1:n.6521T>G
NM_001354579.1:c.6355T>G	NP_001341508.1:p.Ser2119Ala
XR_001740179.2:n.6636T>G
XR_924148.2:n.6642T>G
NM_001184.4:c.6547T>G MANE Select	NP_001175.2:p.Ser2183Ala
NM_001354579.2:c.6355T>G	NP_001341508.1:p.Ser2119Ala