Canonical Allele Identifier: CA546574153

Gene: ATR

Linked Data

• dbSNP Id: rs1559913498
• gnomAD v2: 3-142188735-GAATTAA-G
• gnomAD v3: 3-142469893-GAATTAA-G
• gnomAD v4: 3-142469893-GAATTAA-G
• MyVariant Identifiers: chr3:g.142188736_142188741del (hg19) ; chr3:g.142469894_142469899del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469896_142469901del , CM000665.2:g.142469896_142469901del	GRCh38
NC_000003.11:g.142188738_142188743del , CM000665.1:g.142188738_142188743del	GRCh37
NC_000003.10:g.143671428_143671433del	NCBI36
NG_008951.1:g.113928_113933del

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6319+187_6319+192del MANE Select	ENSP00000343741.4:n.6319+187_6319+192del
ENST00000513291.2:n.1503+187_1503+192del
ENST00000654170.1:n.1162+187_1162+192del
ENST00000656590.1:c.5109+187_5109+192del
ENST00000661310.1:c.6127+187_6127+192del	ENSP00000499589.1:n.6127+187_6127+192del
ENST00000665483.1:n.174+187_174+192del
ENST00000666447.1:n.154+187_154+192del
ENST00000666943.1:n.1783+187_1783+192del
ENST00000350721.8:c.6319+187_6319+192del	ENSP00000343741.4:n.6319+187_6319+192del
NM_001184.3:c.6319+187_6319+192del	NP_001175.2:n.6319+187_6319+192del
XM_011512924.1:c.6325+187_6325+192del	XP_011511226.1:n.6325+187_6325+192del
XM_011512925.1:c.6133+187_6133+192del	XP_011511227.1:n.6133+187_6133+192del
XR_924147.1:n.6414+187_6414+192del
XR_924148.1:n.6414+187_6414+192del
XR_924149.1:n.6293+187_6293+192del
NM_001354579.1:c.6127+187_6127+192del	NP_001341508.1:n.6127+187_6127+192del
XR_001740179.2:n.6408+187_6408+192del
XR_001740180.2:n.6462+187_6462+192del
XR_001740181.2:n.6341+187_6341+192del
XR_001740182.1:n.6293+187_6293+192del
XR_002959543.1:n.6518+187_6518+192del
XR_924148.2:n.6414+187_6414+192del
NM_001184.4:c.6319+187_6319+192del MANE Select	NP_001175.2:n.6319+187_6319+192del
NM_001354579.2:c.6127+187_6127+192del	NP_001341508.1:n.6127+187_6127+192del