Canonical Allele Identifier: CA84734040
Gene: ATR HGNC NCBI

Linked Data

dbSNP Id: rs1032076661

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470468C>T , CM000665.2:g.142470468C>T GRCh38
NC_000003.11:g.142189310C>T , CM000665.1:g.142189310C>T GRCh37
NC_000003.10:g.143672000C>T NCBI36
NG_008951.1:g.113359G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.6222-285G>A MANE Select ENSP00000343741.4:n.6222-285G>A
ENST00000513291.2:n.1406-285G>A
ENST00000654170.1:n.1065-285G>A
ENST00000656590.1:c.5012-285G>A
ENST00000661310.1:c.6030-285G>A ENSP00000499589.1:n.6030-285G>A
ENST00000665483.1:n.77-285G>A
ENST00000666447.1:n.57-285G>A
ENST00000666943.1:n.1686-285G>A
ENST00000350721.8:c.6222-285G>A ENSP00000343741.4:n.6222-285G>A
NM_001184.3:c.6222-285G>A NP_001175.2:n.6222-285G>A
XM_011512924.1:c.6228-285G>A XP_011511226.1:n.6228-285G>A
XM_011512925.1:c.6036-285G>A XP_011511227.1:n.6036-285G>A
XR_924147.1:n.6317-285G>A
XR_924148.1:n.6317-285G>A
XR_924149.1:n.6196-285G>A
NM_001354579.1:c.6030-285G>A NP_001341508.1:n.6030-285G>A
XR_001740179.2:n.6311-285G>A
XR_001740180.2:n.6365-285G>A
XR_001740181.2:n.6244-285G>A
XR_001740182.1:n.6196-285G>A
XR_002959543.1:n.6421-285G>A
XR_924148.2:n.6317-285G>A
NM_001184.4:c.6222-285G>A MANE Select NP_001175.2:n.6222-285G>A
NM_001354579.2:c.6030-285G>A NP_001341508.1:n.6030-285G>A