Canonical Allele Identifier: CA1406991570

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469320_142469321delinsGT , CM000665.2:g.142469320_142469321delinsGT	GRCh38
NC_000003.11:g.142188162_142188163delinsGT , CM000665.1:g.142188162_142188163delinsGT	GRCh37
NC_000003.10:g.143670852_143670853delinsGT	NCBI36
NG_008951.1:g.114506_114507delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6552+16_6552+17delinsAC MANE Select	ENSP00000343741.4:n.6552+16_6552+17delinsAC
ENST00000513291.2:n.1736+16_1736+17delinsAC
ENST00000654170.1:n.1395+16_1395+17delinsAC
ENST00000656590.1:c.5342+16_5342+17delinsAC
ENST00000661310.1:c.6360+16_6360+17delinsAC	ENSP00000499589.1:n.6360+16_6360+17delinsAC
ENST00000665483.1:n.407+16_407+17delinsAC
ENST00000666447.1:n.403_404delinsAC
ENST00000666943.1:n.2032_2033delinsAC
ENST00000350721.8:c.6552+16_6552+17delinsAC	ENSP00000343741.4:n.6552+16_6552+17delinsAC
ENST00000513291.1:c.91+16_91+17delinsAC
NM_001184.3:c.6552+16_6552+17delinsAC	NP_001175.2:n.6552+16_6552+17delinsAC
XM_011512924.1:c.6558+16_6558+17delinsAC	XP_011511226.1:n.6558+16_6558+17delinsAC
XM_011512925.1:c.6366+16_6366+17delinsAC	XP_011511227.1:n.6366+16_6366+17delinsAC
XR_924147.1:n.6647+16_6647+17delinsAC
XR_924148.1:n.6647+16_6647+17delinsAC
XR_924149.1:n.6526+16_6526+17delinsAC
NM_001354579.1:c.6360+16_6360+17delinsAC	NP_001341508.1:n.6360+16_6360+17delinsAC
XR_001740179.2:n.6641+16_6641+17delinsAC
XR_924148.2:n.6647+16_6647+17delinsAC
NM_001184.4:c.6552+16_6552+17delinsAC MANE Select	NP_001175.2:n.6552+16_6552+17delinsAC
NM_001354579.2:c.6360+16_6360+17delinsAC	NP_001341508.1:n.6360+16_6360+17delinsAC