Canonical Allele Identifier: CA354804159

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188195A>C (hg19) ; chr3:g.142469353A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469353A>C , CM000665.2:g.142469353A>C	GRCh38
NC_000003.11:g.142188195A>C , CM000665.1:g.142188195A>C	GRCh37
NC_000003.10:g.143670885A>C	NCBI36
NG_008951.1:g.114474T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6536T>G MANE Select	ENSP00000343741.4:p.Met2179Arg
ENST00000513291.2:n.1720T>G
ENST00000654170.1:n.1379T>G
ENST00000656590.1:c.5326T>G
ENST00000661310.1:c.6344T>G	ENSP00000499589.1:p.Met2115Arg
ENST00000665483.1:n.391T>G
ENST00000666447.1:n.371T>G
ENST00000666943.1:n.2000T>G
ENST00000350721.8:c.6536T>G	ENSP00000343741.4:p.Met2179Arg
ENST00000513291.1:c.75T>G
NM_001184.3:c.6536T>G	NP_001175.2:p.Met2179Arg
XM_011512924.1:c.6542T>G	XP_011511226.1:p.Met2181Arg
XM_011512925.1:c.6350T>G	XP_011511227.1:p.Met2117Arg
XR_924147.1:n.6631T>G
XR_924148.1:n.6631T>G
XR_924149.1:n.6510T>G
NM_001354579.1:c.6344T>G	NP_001341508.1:p.Met2115Arg
XR_001740179.2:n.6625T>G
XR_924148.2:n.6631T>G
NM_001184.4:c.6536T>G MANE Select	NP_001175.2:p.Met2179Arg
NM_001354579.2:c.6344T>G	NP_001341508.1:p.Met2115Arg