Canonical Allele Identifier: CA354793877

Gene: ATR

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.7814C>G MANE Select	ENSP00000343741.4:p.Thr2605Ser
ENST00000513291.2:n.6523C>G
ENST00000653893.1:n.2672C>G
ENST00000654170.1:n.2657C>G
ENST00000656114.1:n.2900C>G
ENST00000656590.1:c.6741C>G
ENST00000658083.1:n.2994C>G
ENST00000661310.1:c.7622C>G	ENSP00000499589.1:p.Thr2541Ser
ENST00000665483.1:n.5354C>G
ENST00000666447.1:n.4317C>G
ENST00000666943.1:n.4546C>G
ENST00000350721.8:c.7814C>G	ENSP00000343741.4:p.Thr2605Ser
ENST00000504521.5:c.403C>G	ENSP00000422553.1:n.403C>G
ENST00000513291.1:c.4878C>G
ENST00000515810.1:c.240C>G	ENSP00000421870.1:n.240C>G
NM_001184.3:c.7814C>G	NP_001175.2:p.Thr2605Ser
XM_011512924.1:c.7820C>G	XP_011511226.1:p.Thr2607Ser
XM_011512925.1:c.7628C>G	XP_011511227.1:p.Thr2543Ser
XR_924147.1:n.10571C>G
XR_924148.1:n.8046C>G
NM_001354579.1:c.7622C>G	NP_001341508.1:p.Thr2541Ser
XR_001740179.2:n.8040C>G
XR_924148.2:n.8046C>G
NM_001184.4:c.7814C>G MANE Select	NP_001175.2:p.Thr2605Ser
NM_001354579.2:c.7622C>G	NP_001341508.1:p.Thr2541Ser