Canonical Allele Identifier: CA354806126

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142189018G>A (hg19) ; chr3:g.142470176G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470176G>A , CM000665.2:g.142470176G>A	GRCh38
NC_000003.11:g.142189018G>A , CM000665.1:g.142189018G>A	GRCh37
NC_000003.10:g.143671708G>A	NCBI36
NG_008951.1:g.113651C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6229C>T MANE Select	ENSP00000343741.4:p.Gln2077Ter
ENST00000513291.2:n.1413C>T
ENST00000654170.1:n.1072C>T
ENST00000656590.1:c.5019C>T
ENST00000661310.1:c.6037C>T	ENSP00000499589.1:p.Gln2013Ter
ENST00000665483.1:n.84C>T
ENST00000666447.1:n.64C>T
ENST00000666943.1:n.1693C>T
ENST00000350721.8:c.6229C>T	ENSP00000343741.4:p.Gln2077Ter
NM_001184.3:c.6229C>T	NP_001175.2:p.Gln2077Ter
XM_011512924.1:c.6235C>T	XP_011511226.1:p.Gln2079Ter
XM_011512925.1:c.6043C>T	XP_011511227.1:p.Gln2015Ter
XR_924147.1:n.6324C>T
XR_924148.1:n.6324C>T
XR_924149.1:n.6203C>T
NM_001354579.1:c.6037C>T	NP_001341508.1:p.Gln2013Ter
XR_001740179.2:n.6318C>T
XR_001740180.2:n.6372C>T
XR_001740181.2:n.6251C>T
XR_001740182.1:n.6203C>T
XR_002959543.1:n.6428C>T
XR_924148.2:n.6324C>T
NM_001184.4:c.6229C>T MANE Select	NP_001175.2:p.Gln2077Ter
NM_001354579.2:c.6037C>T	NP_001341508.1:p.Gln2013Ter