Canonical Allele Identifier: CA436125734

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469451G>A , CM000665.2:g.142469451G>A	GRCh38
NC_000003.11:g.142188293G>A , CM000665.1:g.142188293G>A	GRCh37
NC_000003.10:g.143670983G>A	NCBI36
NG_008951.1:g.114376C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001184.4:c.6438C>T MANE Select	NP_001175.2:p.Ile2146=
ENST00000350721.9:c.6438C>T MANE Select	ENSP00000343741.4:p.Ile2146=
NM_001184.3:c.6438C>T	NP_001175.2:p.Ile2146=
NM_001354579.1:c.6246C>T	NP_001341508.1:p.Ile2082=
NM_001354579.2:c.6246C>T	NP_001341508.1:p.Ile2082=
ENST00000350721.8:c.6438C>T	ENSP00000343741.4:p.Ile2146=
ENST00000513291.2:n.1622C>T
ENST00000654170.1:n.1281C>T
ENST00000656590.1:c.5228C>T
ENST00000661310.1:c.6246C>T	ENSP00000499589.1:p.Ile2082=
ENST00000665483.1:n.293C>T
ENST00000666447.1:n.273C>T
ENST00000666943.1:n.1902C>T
XM_011512924.1:c.6444C>T	XP_011511226.1:p.Ile2148=
XM_011512925.1:c.6252C>T	XP_011511227.1:p.Ile2084=
XR_001740179.2:n.6527C>T
XR_924147.1:n.6533C>T
XR_924148.1:n.6533C>T
XR_924148.2:n.6533C>T
XR_924149.1:n.6412C>T