Canonical Allele Identifier: CA354793986

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168440T>G (hg19) ; chr3:g.142449598T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449598T>G , CM000665.2:g.142449598T>G	GRCh38
NC_000003.11:g.142168440T>G , CM000665.1:g.142168440T>G	GRCh37
NC_000003.10:g.143651130T>G	NCBI36
NG_008951.1:g.134229A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7766A>C MANE Select	ENSP00000343741.4:p.Lys2589Thr
ENST00000513291.2:n.6475A>C
ENST00000653893.1:n.2624A>C
ENST00000654170.1:n.2609A>C
ENST00000656114.1:n.2852A>C
ENST00000656590.1:c.6693A>C
ENST00000658083.1:n.2946A>C
ENST00000661310.1:c.7574A>C	ENSP00000499589.1:p.Lys2525Thr
ENST00000665483.1:n.5306A>C
ENST00000666447.1:n.4269A>C
ENST00000666943.1:n.4498A>C
ENST00000350721.8:c.7766A>C	ENSP00000343741.4:p.Lys2589Thr
ENST00000504521.5:c.355A>C	ENSP00000422553.1:n.355A>C
ENST00000513291.1:c.4830A>C
ENST00000515810.1:c.192A>C	ENSP00000421870.1:n.192A>C
NM_001184.3:c.7766A>C	NP_001175.2:p.Lys2589Thr
XM_011512924.1:c.7772A>C	XP_011511226.1:p.Lys2591Thr
XM_011512925.1:c.7580A>C	XP_011511227.1:p.Lys2527Thr
XR_924147.1:n.10523A>C
XR_924148.1:n.7998A>C
NM_001354579.1:c.7574A>C	NP_001341508.1:p.Lys2525Thr
XR_001740179.2:n.7992A>C
XR_924148.2:n.7998A>C
NM_001184.4:c.7766A>C MANE Select	NP_001175.2:p.Lys2589Thr
NM_001354579.2:c.7574A>C	NP_001341508.1:p.Lys2525Thr