Canonical Allele Identifier: CA2704280848

Gene: ATR

Linked Data

• dbSNP Id: rs2108463183

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553445_142553446insTC , CM000665.2:g.142553445_142553446insTC	GRCh38
NC_000003.11:g.142272287_142272288insTC , CM000665.1:g.142272287_142272288insTC	GRCh37
NC_000003.10:g.143754977_143754978insTC	NCBI36
NG_008951.1:g.30382_30383insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2634-47_2634-46insAG MANE Select	ENSP00000343741.4:n.2634-47_2634-46insAG
ENST00000515149.3:c.*1408-47_*1408-46insAG	ENSP00000425897.3:n.*1408-47_*1408-46insAG
ENST00000653868.1:n.2663-47_2663-46insAG
ENST00000656590.1:c.1424-47_1424-46insAG
ENST00000659195.1:n.5509-47_5509-46insAG
ENST00000661310.1:c.2442-47_2442-46insAG	ENSP00000499589.1:n.2442-47_2442-46insAG
ENST00000350721.8:c.2634-47_2634-46insAG	ENSP00000343741.4:n.2634-47_2634-46insAG
NM_001184.3:c.2634-47_2634-46insAG	NP_001175.2:n.2634-47_2634-46insAG
XM_011512924.1:c.2634-47_2634-46insAG	XP_011511226.1:n.2634-47_2634-46insAG
XM_011512925.1:c.2442-47_2442-46insAG	XP_011511227.1:n.2442-47_2442-46insAG
XM_011512926.1:c.2634-47_2634-46insAG	XP_011511228.1:n.2634-47_2634-46insAG
XM_011512927.1:c.2634-47_2634-46insAG	XP_011511229.1:n.2634-47_2634-46insAG
XR_924147.1:n.2723-47_2723-46insAG
XR_924148.1:n.2723-47_2723-46insAG
XR_924149.1:n.2723-47_2723-46insAG
NM_001354579.1:c.2442-47_2442-46insAG	NP_001341508.1:n.2442-47_2442-46insAG
XR_001740179.2:n.2723-47_2723-46insAG
XR_001740180.2:n.2723-47_2723-46insAG
XR_001740181.2:n.2723-47_2723-46insAG
XR_001740182.1:n.2723-47_2723-46insAG
XR_002959543.1:n.2723-47_2723-46insAG
XR_924148.2:n.2723-47_2723-46insAG
NM_001184.4:c.2634-47_2634-46insAG MANE Select	NP_001175.2:n.2634-47_2634-46insAG
NM_001354579.2:c.2442-47_2442-46insAG	NP_001341508.1:n.2442-47_2442-46insAG