Canonical Allele Identifier: CA354793876

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168392G>A (hg19) ; chr3:g.142449550G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449550G>A , CM000665.2:g.142449550G>A	GRCh38
NC_000003.11:g.142168392G>A , CM000665.1:g.142168392G>A	GRCh37
NC_000003.10:g.143651082G>A	NCBI36
NG_008951.1:g.134277C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.7814C>T MANE Select	ENSP00000343741.4:p.Thr2605Ile
ENST00000513291.2:n.6523C>T
ENST00000653893.1:n.2672C>T
ENST00000654170.1:n.2657C>T
ENST00000656114.1:n.2900C>T
ENST00000656590.1:c.6741C>T
ENST00000658083.1:n.2994C>T
ENST00000661310.1:c.7622C>T	ENSP00000499589.1:p.Thr2541Ile
ENST00000665483.1:n.5354C>T
ENST00000666447.1:n.4317C>T
ENST00000666943.1:n.4546C>T
ENST00000350721.8:c.7814C>T	ENSP00000343741.4:p.Thr2605Ile
ENST00000504521.5:c.403C>T	ENSP00000422553.1:n.403C>T
ENST00000513291.1:c.4878C>T
ENST00000515810.1:c.240C>T	ENSP00000421870.1:n.240C>T
NM_001184.3:c.7814C>T	NP_001175.2:p.Thr2605Ile
XM_011512924.1:c.7820C>T	XP_011511226.1:p.Thr2607Ile
XM_011512925.1:c.7628C>T	XP_011511227.1:p.Thr2543Ile
XR_924147.1:n.10571C>T
XR_924148.1:n.8046C>T
NM_001354579.1:c.7622C>T	NP_001341508.1:p.Thr2541Ile
XR_001740179.2:n.8040C>T
XR_924148.2:n.8046C>T
NM_001184.4:c.7814C>T MANE Select	NP_001175.2:p.Thr2605Ile
NM_001354579.2:c.7622C>T	NP_001341508.1:p.Thr2541Ile