Canonical Allele Identifier: CA2520552875

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469911_142469912insGCTATTTTTAA , CM000665.2:g.142469911_142469912insGCTATTTTTAA	GRCh38
NC_000003.11:g.142188753_142188754insGCTATTTTTAA , CM000665.1:g.142188753_142188754insGCTATTTTTAA	GRCh37
NC_000003.10:g.143671443_143671444insGCTATTTTTAA	NCBI36
NG_008951.1:g.113917_113918insAAAAATAGCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6319+176_6319+177insAAAAATAGCTT MANE Select	ENSP00000343741.4:n.6319+176_6319+177insAAAAATAGCTT
ENST00000513291.2:n.1503+176_1503+177insAAAAATAGCTT
ENST00000654170.1:n.1162+176_1162+177insAAAAATAGCTT
ENST00000656590.1:c.5109+176_5109+177insAAAAATAGCTT
ENST00000661310.1:c.6127+176_6127+177insAAAAATAGCTT	ENSP00000499589.1:n.6127+176_6127+177insAAAAATAGCTT
ENST00000665483.1:n.174+176_174+177insAAAAATAGCTT
ENST00000666447.1:n.154+176_154+177insAAAAATAGCTT
ENST00000666943.1:n.1783+176_1783+177insAAAAATAGCTT
ENST00000350721.8:c.6319+176_6319+177insAAAAATAGCTT	ENSP00000343741.4:n.6319+176_6319+177insAAAAATAGCTT
NM_001184.3:c.6319+176_6319+177insAAAAATAGCTT	NP_001175.2:n.6319+176_6319+177insAAAAATAGCTT
XM_011512924.1:c.6325+176_6325+177insAAAAATAGCTT	XP_011511226.1:n.6325+176_6325+177insAAAAATAGCTT
XM_011512925.1:c.6133+176_6133+177insAAAAATAGCTT	XP_011511227.1:n.6133+176_6133+177insAAAAATAGCTT
XR_924147.1:n.6414+176_6414+177insAAAAATAGCTT
XR_924148.1:n.6414+176_6414+177insAAAAATAGCTT
XR_924149.1:n.6293+176_6293+177insAAAAATAGCTT
NM_001354579.1:c.6127+176_6127+177insAAAAATAGCTT	NP_001341508.1:n.6127+176_6127+177insAAAAATAGCTT
XR_001740179.2:n.6408+176_6408+177insAAAAATAGCTT
XR_001740180.2:n.6462+176_6462+177insAAAAATAGCTT
XR_001740181.2:n.6341+176_6341+177insAAAAATAGCTT
XR_001740182.1:n.6293+176_6293+177insAAAAATAGCTT
XR_002959543.1:n.6518+176_6518+177insAAAAATAGCTT
XR_924148.2:n.6414+176_6414+177insAAAAATAGCTT
NM_001184.4:c.6319+176_6319+177insAAAAATAGCTT MANE Select	NP_001175.2:n.6319+176_6319+177insAAAAATAGCTT
NM_001354579.2:c.6127+176_6127+177insAAAAATAGCTT	NP_001341508.1:n.6127+176_6127+177insAAAAATAGCTT