Canonical Allele Identifier: CA354793962

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168431A>C (hg19) ; chr3:g.142449589A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449589A>C , CM000665.2:g.142449589A>C	GRCh38
NC_000003.11:g.142168431A>C , CM000665.1:g.142168431A>C	GRCh37
NC_000003.10:g.143651121A>C	NCBI36
NG_008951.1:g.134238T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7775T>G MANE Select	ENSP00000343741.4:p.Val2592Gly
ENST00000513291.2:n.6484T>G
ENST00000653893.1:n.2633T>G
ENST00000654170.1:n.2618T>G
ENST00000656114.1:n.2861T>G
ENST00000656590.1:c.6702T>G
ENST00000658083.1:n.2955T>G
ENST00000661310.1:c.7583T>G	ENSP00000499589.1:p.Val2528Gly
ENST00000665483.1:n.5315T>G
ENST00000666447.1:n.4278T>G
ENST00000666943.1:n.4507T>G
ENST00000350721.8:c.7775T>G	ENSP00000343741.4:p.Val2592Gly
ENST00000504521.5:c.364T>G	ENSP00000422553.1:n.364T>G
ENST00000513291.1:c.4839T>G
ENST00000515810.1:c.201T>G	ENSP00000421870.1:n.201T>G
NM_001184.3:c.7775T>G	NP_001175.2:p.Val2592Gly
XM_011512924.1:c.7781T>G	XP_011511226.1:p.Val2594Gly
XM_011512925.1:c.7589T>G	XP_011511227.1:p.Val2530Gly
XR_924147.1:n.10532T>G
XR_924148.1:n.8007T>G
NM_001354579.1:c.7583T>G	NP_001341508.1:p.Val2528Gly
XR_001740179.2:n.8001T>G
XR_924148.2:n.8007T>G
NM_001184.4:c.7775T>G MANE Select	NP_001175.2:p.Val2592Gly
NM_001354579.2:c.7583T>G	NP_001341508.1:p.Val2528Gly