Canonical Allele Identifier: CA354793949

Gene: ATR

Linked Data

• COSMIC: COSM6262303
• MyVariant Identifiers: chr3:g.142168424G>T (hg19) ; chr3:g.142449582G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449582G>T , CM000665.2:g.142449582G>T	GRCh38
NC_000003.11:g.142168424G>T , CM000665.1:g.142168424G>T	GRCh37
NC_000003.10:g.143651114G>T	NCBI36
NG_008951.1:g.134245C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7782C>A MANE Select	ENSP00000343741.4:p.Asp2594Glu
ENST00000513291.2:n.6491C>A
ENST00000653893.1:n.2640C>A
ENST00000654170.1:n.2625C>A
ENST00000656114.1:n.2868C>A
ENST00000656590.1:c.6709C>A
ENST00000658083.1:n.2962C>A
ENST00000661310.1:c.7590C>A	ENSP00000499589.1:p.Asp2530Glu
ENST00000665483.1:n.5322C>A
ENST00000666447.1:n.4285C>A
ENST00000666943.1:n.4514C>A
ENST00000350721.8:c.7782C>A	ENSP00000343741.4:p.Asp2594Glu
ENST00000504521.5:c.371C>A	ENSP00000422553.1:n.371C>A
ENST00000513291.1:c.4846C>A
ENST00000515810.1:c.208C>A	ENSP00000421870.1:n.208C>A
NM_001184.3:c.7782C>A	NP_001175.2:p.Asp2594Glu
XM_011512924.1:c.7788C>A	XP_011511226.1:p.Asp2596Glu
XM_011512925.1:c.7596C>A	XP_011511227.1:p.Asp2532Glu
XR_924147.1:n.10539C>A
XR_924148.1:n.8014C>A
NM_001354579.1:c.7590C>A	NP_001341508.1:p.Asp2530Glu
XR_001740179.2:n.8008C>A
XR_924148.2:n.8014C>A
NM_001184.4:c.7782C>A MANE Select	NP_001175.2:p.Asp2594Glu
NM_001354579.2:c.7590C>A	NP_001341508.1:p.Asp2530Glu