Canonical Allele Identifier: CA354793966

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168432C>T (hg19) ; chr3:g.142449590C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449590C>T , CM000665.2:g.142449590C>T	GRCh38
NC_000003.11:g.142168432C>T , CM000665.1:g.142168432C>T	GRCh37
NC_000003.10:g.143651122C>T	NCBI36
NG_008951.1:g.134237G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7774G>A MANE Select	ENSP00000343741.4:p.Val2592Ile
ENST00000513291.2:n.6483G>A
ENST00000653893.1:n.2632G>A
ENST00000654170.1:n.2617G>A
ENST00000656114.1:n.2860G>A
ENST00000656590.1:c.6701G>A
ENST00000658083.1:n.2954G>A
ENST00000661310.1:c.7582G>A	ENSP00000499589.1:p.Val2528Ile
ENST00000665483.1:n.5314G>A
ENST00000666447.1:n.4277G>A
ENST00000666943.1:n.4506G>A
ENST00000350721.8:c.7774G>A	ENSP00000343741.4:p.Val2592Ile
ENST00000504521.5:c.363G>A	ENSP00000422553.1:n.363G>A
ENST00000513291.1:c.4838G>A
ENST00000515810.1:c.200G>A	ENSP00000421870.1:n.200G>A
NM_001184.3:c.7774G>A	NP_001175.2:p.Val2592Ile
XM_011512924.1:c.7780G>A	XP_011511226.1:p.Val2594Ile
XM_011512925.1:c.7588G>A	XP_011511227.1:p.Val2530Ile
XR_924147.1:n.10531G>A
XR_924148.1:n.8006G>A
NM_001354579.1:c.7582G>A	NP_001341508.1:p.Val2528Ile
XR_001740179.2:n.8000G>A
XR_924148.2:n.8006G>A
NM_001184.4:c.7774G>A MANE Select	NP_001175.2:p.Val2592Ile
NM_001354579.2:c.7582G>A	NP_001341508.1:p.Val2528Ile