Canonical Allele Identifier: CA16604477

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142465255G>A , CM000665.2:g.142465255G>A	GRCh38
NC_000003.11:g.142184097G>A , CM000665.1:g.142184097G>A	GRCh37
NC_000003.10:g.143666787G>A	NCBI36
NG_008951.1:g.118572C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001184.4:c.6898-15C>T MANE Select	NP_001175.2:n.6898-15C>T
ENST00000350721.9:c.6898-15C>T MANE Select	ENSP00000343741.4:n.6898-15C>T
NM_001184.3:c.6898-15C>T	NP_001175.2:n.6898-15C>T
NM_001354579.1:c.6706-15C>T	NP_001341508.1:n.6706-15C>T
NM_001354579.2:c.6706-15C>T	NP_001341508.1:n.6706-15C>T
ENST00000350721.8:c.6898-15C>T	ENSP00000343741.4:n.6898-15C>T
ENST00000513291.1:c.437-15C>T
ENST00000513291.2:n.2082-15C>T
ENST00000654170.1:n.1741-15C>T
ENST00000656590.1:c.5688-15C>T
ENST00000661310.1:c.6706-15C>T	ENSP00000499589.1:n.6706-15C>T
ENST00000665483.1:n.3221C>T
ENST00000666447.1:n.3401-15C>T
ENST00000666943.1:n.3630-15C>T
XM_011512924.1:c.6904-15C>T	XP_011511226.1:n.6904-15C>T
XM_011512925.1:c.6712-15C>T	XP_011511227.1:n.6712-15C>T
XR_001740179.2:n.6987-15C>T
XR_924147.1:n.6993-15C>T
XR_924148.1:n.6993-15C>T
XR_924148.2:n.6993-15C>T