Canonical Allele Identifier: CA1406991800

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469908_142469909delinsTA , CM000665.2:g.142469908_142469909delinsTA	GRCh38
NC_000003.11:g.142188750_142188751delinsTA , CM000665.1:g.142188750_142188751delinsTA	GRCh37
NC_000003.10:g.143671440_143671441delinsTA	NCBI36
NG_008951.1:g.113918_113919delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6319+177_6319+178delinsTA MANE Select	ENSP00000343741.4:n.6319+177_6319+178delinsTA
ENST00000513291.2:n.1503+177_1503+178delinsTA
ENST00000654170.1:n.1162+177_1162+178delinsTA
ENST00000656590.1:c.5109+177_5109+178delinsTA
ENST00000661310.1:c.6127+177_6127+178delinsTA	ENSP00000499589.1:n.6127+177_6127+178delinsTA
ENST00000665483.1:n.174+177_174+178delinsTA
ENST00000666447.1:n.154+177_154+178delinsTA
ENST00000666943.1:n.1783+177_1783+178delinsTA
ENST00000350721.8:c.6319+177_6319+178delinsTA	ENSP00000343741.4:n.6319+177_6319+178delinsTA
NM_001184.3:c.6319+177_6319+178delinsTA	NP_001175.2:n.6319+177_6319+178delinsTA
XM_011512924.1:c.6325+177_6325+178delinsTA	XP_011511226.1:n.6325+177_6325+178delinsTA
XM_011512925.1:c.6133+177_6133+178delinsTA	XP_011511227.1:n.6133+177_6133+178delinsTA
XR_924147.1:n.6414+177_6414+178delinsTA
XR_924148.1:n.6414+177_6414+178delinsTA
XR_924149.1:n.6293+177_6293+178delinsTA
NM_001354579.1:c.6127+177_6127+178delinsTA	NP_001341508.1:n.6127+177_6127+178delinsTA
XR_001740179.2:n.6408+177_6408+178delinsTA
XR_001740180.2:n.6462+177_6462+178delinsTA
XR_001740181.2:n.6341+177_6341+178delinsTA
XR_001740182.1:n.6293+177_6293+178delinsTA
XR_002959543.1:n.6518+177_6518+178delinsTA
XR_924148.2:n.6414+177_6414+178delinsTA
NM_001184.4:c.6319+177_6319+178delinsTA MANE Select	NP_001175.2:n.6319+177_6319+178delinsTA
NM_001354579.2:c.6127+177_6127+178delinsTA	NP_001341508.1:n.6127+177_6127+178delinsTA