Canonical Allele Identifier: CA354793905

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168405C>A (hg19) ; chr3:g.142449563C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449563C>A , CM000665.2:g.142449563C>A	GRCh38
NC_000003.11:g.142168405C>A , CM000665.1:g.142168405C>A	GRCh37
NC_000003.10:g.143651095C>A	NCBI36
NG_008951.1:g.134264G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7801G>T MANE Select	ENSP00000343741.4:p.Gly2601Cys
ENST00000513291.2:n.6510G>T
ENST00000653893.1:n.2659G>T
ENST00000654170.1:n.2644G>T
ENST00000656114.1:n.2887G>T
ENST00000656590.1:c.6728G>T
ENST00000658083.1:n.2981G>T
ENST00000661310.1:c.7609G>T	ENSP00000499589.1:p.Gly2537Cys
ENST00000665483.1:n.5341G>T
ENST00000666447.1:n.4304G>T
ENST00000666943.1:n.4533G>T
ENST00000350721.8:c.7801G>T	ENSP00000343741.4:p.Gly2601Cys
ENST00000504521.5:c.390G>T	ENSP00000422553.1:n.390G>T
ENST00000513291.1:c.4865G>T
ENST00000515810.1:c.227G>T	ENSP00000421870.1:n.227G>T
NM_001184.3:c.7801G>T	NP_001175.2:p.Gly2601Cys
XM_011512924.1:c.7807G>T	XP_011511226.1:p.Gly2603Cys
XM_011512925.1:c.7615G>T	XP_011511227.1:p.Gly2539Cys
XR_924147.1:n.10558G>T
XR_924148.1:n.8033G>T
NM_001354579.1:c.7609G>T	NP_001341508.1:p.Gly2537Cys
XR_001740179.2:n.8027G>T
XR_924148.2:n.8033G>T
NM_001184.4:c.7801G>T MANE Select	NP_001175.2:p.Gly2601Cys
NM_001354579.2:c.7609G>T	NP_001341508.1:p.Gly2537Cys