Canonical Allele Identifier: CA436107415

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168436G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449594G>C , CM000665.2:g.142449594G>C	GRCh38
NC_000003.11:g.142168436G>C , CM000665.1:g.142168436G>C	GRCh37
NC_000003.10:g.143651126G>C	NCBI36
NG_008951.1:g.134233C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7770C>G MANE Select	ENSP00000343741.4:p.Thr2590=
ENST00000513291.2:n.6479C>G
ENST00000653893.1:n.2628C>G
ENST00000654170.1:n.2613C>G
ENST00000656114.1:n.2856C>G
ENST00000656590.1:c.6697C>G
ENST00000658083.1:n.2950C>G
ENST00000661310.1:c.7578C>G	ENSP00000499589.1:p.Thr2526=
ENST00000665483.1:n.5310C>G
ENST00000666447.1:n.4273C>G
ENST00000666943.1:n.4502C>G
ENST00000350721.8:c.7770C>G	ENSP00000343741.4:p.Thr2590=
ENST00000504521.5:c.359C>G	ENSP00000422553.1:n.359C>G
ENST00000513291.1:c.4834C>G
ENST00000515810.1:c.196C>G	ENSP00000421870.1:n.196C>G
NM_001184.3:c.7770C>G	NP_001175.2:p.Thr2590=
XM_011512924.1:c.7776C>G	XP_011511226.1:p.Thr2592=
XM_011512925.1:c.7584C>G	XP_011511227.1:p.Thr2528=
XR_924147.1:n.10527C>G
XR_924148.1:n.8002C>G
NM_001354579.1:c.7578C>G	NP_001341508.1:p.Thr2526=
XR_001740179.2:n.7996C>G
XR_924148.2:n.8002C>G
NM_001184.4:c.7770C>G MANE Select	NP_001175.2:p.Thr2590=
NM_001354579.2:c.7578C>G	NP_001341508.1:p.Thr2526=