Canonical Allele Identifier: CA1406991836

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470009_142470010delinsGA , CM000665.2:g.142470009_142470010delinsGA	GRCh38
NC_000003.11:g.142188851_142188852delinsGA , CM000665.1:g.142188851_142188852delinsGA	GRCh37
NC_000003.10:g.143671541_143671542delinsGA	NCBI36
NG_008951.1:g.113817_113818delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6319+76_6319+77delinsTC MANE Select	ENSP00000343741.4:n.6319+76_6319+77delinsTC
ENST00000513291.2:n.1503+76_1503+77delinsTC
ENST00000654170.1:n.1162+76_1162+77delinsTC
ENST00000656590.1:c.5109+76_5109+77delinsTC
ENST00000661310.1:c.6127+76_6127+77delinsTC	ENSP00000499589.1:n.6127+76_6127+77delinsTC
ENST00000665483.1:n.174+76_174+77delinsTC
ENST00000666447.1:n.154+76_154+77delinsTC
ENST00000666943.1:n.1783+76_1783+77delinsTC
ENST00000350721.8:c.6319+76_6319+77delinsTC	ENSP00000343741.4:n.6319+76_6319+77delinsTC
NM_001184.3:c.6319+76_6319+77delinsTC	NP_001175.2:n.6319+76_6319+77delinsTC
XM_011512924.1:c.6325+76_6325+77delinsTC	XP_011511226.1:n.6325+76_6325+77delinsTC
XM_011512925.1:c.6133+76_6133+77delinsTC	XP_011511227.1:n.6133+76_6133+77delinsTC
XR_924147.1:n.6414+76_6414+77delinsTC
XR_924148.1:n.6414+76_6414+77delinsTC
XR_924149.1:n.6293+76_6293+77delinsTC
NM_001354579.1:c.6127+76_6127+77delinsTC	NP_001341508.1:n.6127+76_6127+77delinsTC
XR_001740179.2:n.6408+76_6408+77delinsTC
XR_001740180.2:n.6462+76_6462+77delinsTC
XR_001740181.2:n.6341+76_6341+77delinsTC
XR_001740182.1:n.6293+76_6293+77delinsTC
XR_002959543.1:n.6518+76_6518+77delinsTC
XR_924148.2:n.6414+76_6414+77delinsTC
NM_001184.4:c.6319+76_6319+77delinsTC MANE Select	NP_001175.2:n.6319+76_6319+77delinsTC
NM_001354579.2:c.6127+76_6127+77delinsTC	NP_001341508.1:n.6127+76_6127+77delinsTC