Canonical Allele Identifier: CA354793680

Gene: ATR

Linked Data

• COSMIC: COSM1308679
• MyVariant Identifiers: chr3:g.142168301C>G (hg19) ; chr3:g.142449459C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449459C>G , CM000665.2:g.142449459C>G	GRCh38
NC_000003.11:g.142168301C>G , CM000665.1:g.142168301C>G	GRCh37
NC_000003.10:g.143650991C>G	NCBI36
NG_008951.1:g.134368G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7905G>C MANE Select	ENSP00000343741.4:p.Gln2635His
ENST00000513291.2:n.6614G>C
ENST00000653893.1:n.2763G>C
ENST00000654170.1:n.2748G>C
ENST00000656114.1:n.2991G>C
ENST00000656590.1:c.6832G>C
ENST00000658083.1:n.3085G>C
ENST00000661310.1:c.7713G>C	ENSP00000499589.1:p.Gln2571His
ENST00000665483.1:n.5445G>C
ENST00000666447.1:n.4408G>C
ENST00000666943.1:n.4637G>C
ENST00000350721.8:c.7905G>C	ENSP00000343741.4:p.Gln2635His
ENST00000504521.5:c.494G>C	ENSP00000422553.1:n.494G>C
ENST00000513291.1:c.4969G>C
ENST00000515810.1:c.331G>C	ENSP00000421870.1:n.331G>C
NM_001184.3:c.7905G>C	NP_001175.2:p.Gln2635His
XM_011512924.1:c.7911G>C	XP_011511226.1:p.Gln2637His
XM_011512925.1:c.7719G>C	XP_011511227.1:p.Gln2573His
XR_924147.1:n.10662G>C
XR_924148.1:n.8137G>C
NM_001354579.1:c.7713G>C	NP_001341508.1:p.Gln2571His
XR_001740179.2:n.8131G>C
XR_924148.2:n.8137G>C
NM_001184.4:c.7905G>C MANE Select	NP_001175.2:p.Gln2635His
NM_001354579.2:c.7713G>C	NP_001341508.1:p.Gln2571His