Canonical Allele Identifier: CA354793860

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168383C>A (hg19) ; chr3:g.142449541C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449541C>A , CM000665.2:g.142449541C>A	GRCh38
NC_000003.11:g.142168383C>A , CM000665.1:g.142168383C>A	GRCh37
NC_000003.10:g.143651073C>A	NCBI36
NG_008951.1:g.134286G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7823G>T MANE Select	ENSP00000343741.4:p.Arg2608Ile
ENST00000513291.2:n.6532G>T
ENST00000653893.1:n.2681G>T
ENST00000654170.1:n.2666G>T
ENST00000656114.1:n.2909G>T
ENST00000656590.1:c.6750G>T
ENST00000658083.1:n.3003G>T
ENST00000661310.1:c.7631G>T	ENSP00000499589.1:p.Arg2544Ile
ENST00000665483.1:n.5363G>T
ENST00000666447.1:n.4326G>T
ENST00000666943.1:n.4555G>T
ENST00000350721.8:c.7823G>T	ENSP00000343741.4:p.Arg2608Ile
ENST00000504521.5:c.412G>T	ENSP00000422553.1:n.412G>T
ENST00000513291.1:c.4887G>T
ENST00000515810.1:c.249G>T	ENSP00000421870.1:n.249G>T
NM_001184.3:c.7823G>T	NP_001175.2:p.Arg2608Ile
XM_011512924.1:c.7829G>T	XP_011511226.1:p.Arg2610Ile
XM_011512925.1:c.7637G>T	XP_011511227.1:p.Arg2546Ile
XR_924147.1:n.10580G>T
XR_924148.1:n.8055G>T
NM_001354579.1:c.7631G>T	NP_001341508.1:p.Arg2544Ile
XR_001740179.2:n.8049G>T
XR_924148.2:n.8055G>T
NM_001184.4:c.7823G>T MANE Select	NP_001175.2:p.Arg2608Ile
NM_001354579.2:c.7631G>T	NP_001341508.1:p.Arg2544Ile