Canonical Allele Identifier: CA2704281336

Gene: ATR

Linked Data

• dbSNP Id: rs2108278266

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469284C>G , CM000665.2:g.142469284C>G	GRCh38
NC_000003.11:g.142188126C>G , CM000665.1:g.142188126C>G	GRCh37
NC_000003.10:g.143670816C>G	NCBI36
NG_008951.1:g.114543G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6552+53G>C MANE Select	ENSP00000343741.4:n.6552+53G>C
ENST00000513291.2:n.1736+53G>C
ENST00000654170.1:n.1395+53G>C
ENST00000656590.1:c.5342+53G>C
ENST00000661310.1:c.6360+53G>C	ENSP00000499589.1:n.6360+53G>C
ENST00000665483.1:n.407+53G>C
ENST00000666447.1:n.440G>C
ENST00000666943.1:n.2069G>C
ENST00000350721.8:c.6552+53G>C	ENSP00000343741.4:n.6552+53G>C
ENST00000513291.1:c.91+53G>C
NM_001184.3:c.6552+53G>C	NP_001175.2:n.6552+53G>C
XM_011512924.1:c.6558+53G>C	XP_011511226.1:n.6558+53G>C
XM_011512925.1:c.6366+53G>C	XP_011511227.1:n.6366+53G>C
XR_924147.1:n.6647+53G>C
XR_924148.1:n.6647+53G>C
XR_924149.1:n.6526+53G>C
NM_001354579.1:c.6360+53G>C	NP_001341508.1:n.6360+53G>C
XR_001740179.2:n.6641+53G>C
XR_924148.2:n.6647+53G>C
NM_001184.4:c.6552+53G>C MANE Select	NP_001175.2:n.6552+53G>C
NM_001354579.2:c.6360+53G>C	NP_001341508.1:n.6360+53G>C