Canonical Allele Identifier: CA354793883

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168394C>G (hg19) ; chr3:g.142449552C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449552C>G , CM000665.2:g.142449552C>G	GRCh38
NC_000003.11:g.142168394C>G , CM000665.1:g.142168394C>G	GRCh37
NC_000003.10:g.143651084C>G	NCBI36
NG_008951.1:g.134275G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.7812G>C MANE Select	ENSP00000343741.4:p.Lys2604Asn
ENST00000513291.2:n.6521G>C
ENST00000653893.1:n.2670G>C
ENST00000654170.1:n.2655G>C
ENST00000656114.1:n.2898G>C
ENST00000656590.1:c.6739G>C
ENST00000658083.1:n.2992G>C
ENST00000661310.1:c.7620G>C	ENSP00000499589.1:p.Lys2540Asn
ENST00000665483.1:n.5352G>C
ENST00000666447.1:n.4315G>C
ENST00000666943.1:n.4544G>C
ENST00000350721.8:c.7812G>C	ENSP00000343741.4:p.Lys2604Asn
ENST00000504521.5:c.401G>C	ENSP00000422553.1:n.401G>C
ENST00000513291.1:c.4876G>C
ENST00000515810.1:c.238G>C	ENSP00000421870.1:n.238G>C
NM_001184.3:c.7812G>C	NP_001175.2:p.Lys2604Asn
XM_011512924.1:c.7818G>C	XP_011511226.1:p.Lys2606Asn
XM_011512925.1:c.7626G>C	XP_011511227.1:p.Lys2542Asn
XR_924147.1:n.10569G>C
XR_924148.1:n.8044G>C
NM_001354579.1:c.7620G>C	NP_001341508.1:p.Lys2540Asn
XR_001740179.2:n.8038G>C
XR_924148.2:n.8044G>C
NM_001184.4:c.7812G>C MANE Select	NP_001175.2:p.Lys2604Asn
NM_001354579.2:c.7620G>C	NP_001341508.1:p.Lys2540Asn