Canonical Allele Identifier: CA354793901

Gene: ATR

Linked Data

• dbSNP Id: rs2108242521
• MyVariant Identifiers: chr3:g.142168402C>T (hg19) ; chr3:g.142449560C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449560C>T , CM000665.2:g.142449560C>T	GRCh38
NC_000003.11:g.142168402C>T , CM000665.1:g.142168402C>T	GRCh37
NC_000003.10:g.143651092C>T	NCBI36
NG_008951.1:g.134267G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.7804G>A MANE Select	ENSP00000343741.4:p.Val2602Ile
ENST00000513291.2:n.6513G>A
ENST00000653893.1:n.2662G>A
ENST00000654170.1:n.2647G>A
ENST00000656114.1:n.2890G>A
ENST00000656590.1:c.6731G>A
ENST00000658083.1:n.2984G>A
ENST00000661310.1:c.7612G>A	ENSP00000499589.1:p.Val2538Ile
ENST00000665483.1:n.5344G>A
ENST00000666447.1:n.4307G>A
ENST00000666943.1:n.4536G>A
ENST00000350721.8:c.7804G>A	ENSP00000343741.4:p.Val2602Ile
ENST00000504521.5:c.393G>A	ENSP00000422553.1:n.393G>A
ENST00000513291.1:c.4868G>A
ENST00000515810.1:c.230G>A	ENSP00000421870.1:n.230G>A
NM_001184.3:c.7804G>A	NP_001175.2:p.Val2602Ile
XM_011512924.1:c.7810G>A	XP_011511226.1:p.Val2604Ile
XM_011512925.1:c.7618G>A	XP_011511227.1:p.Val2540Ile
XR_924147.1:n.10561G>A
XR_924148.1:n.8036G>A
NM_001354579.1:c.7612G>A	NP_001341508.1:p.Val2538Ile
XR_001740179.2:n.8030G>A
XR_924148.2:n.8036G>A
NM_001184.4:c.7804G>A MANE Select	NP_001175.2:p.Val2602Ile
NM_001354579.2:c.7612G>A	NP_001341508.1:p.Val2538Ile