Canonical Allele Identifier: CA354805550

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188942T>A (hg19) ; chr3:g.142470100T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470100T>A , CM000665.2:g.142470100T>A	GRCh38
NC_000003.11:g.142188942T>A , CM000665.1:g.142188942T>A	GRCh37
NC_000003.10:g.143671632T>A	NCBI36
NG_008951.1:g.113727A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6305A>T MANE Select	ENSP00000343741.4:p.Tyr2102Phe
ENST00000513291.2:n.1489A>T
ENST00000654170.1:n.1148A>T
ENST00000656590.1:c.5095A>T
ENST00000661310.1:c.6113A>T	ENSP00000499589.1:p.Tyr2038Phe
ENST00000665483.1:n.160A>T
ENST00000666447.1:n.140A>T
ENST00000666943.1:n.1769A>T
ENST00000350721.8:c.6305A>T	ENSP00000343741.4:p.Tyr2102Phe
NM_001184.3:c.6305A>T	NP_001175.2:p.Tyr2102Phe
XM_011512924.1:c.6311A>T	XP_011511226.1:p.Tyr2104Phe
XM_011512925.1:c.6119A>T	XP_011511227.1:p.Tyr2040Phe
XR_924147.1:n.6400A>T
XR_924148.1:n.6400A>T
XR_924149.1:n.6279A>T
NM_001354579.1:c.6113A>T	NP_001341508.1:p.Tyr2038Phe
XR_001740179.2:n.6394A>T
XR_001740180.2:n.6448A>T
XR_001740181.2:n.6327A>T
XR_001740182.1:n.6279A>T
XR_002959543.1:n.6504A>T
XR_924148.2:n.6400A>T
NM_001184.4:c.6305A>T MANE Select	NP_001175.2:p.Tyr2102Phe
NM_001354579.2:c.6113A>T	NP_001341508.1:p.Tyr2038Phe