Canonical Allele Identifier: CA349814
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 219697
dbSNP Id: rs864622212

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95506544_95506545del , CM000671.2:g.95506544_95506545del GRCh38
NC_000009.11:g.98268826_98268827del , CM000671.1:g.98268826_98268827del GRCh37
NC_000009.10:g.97308647_97308648del NCBI36
NG_007664.1:g.15423_15424del , LRG_515:g.15423_15424del

Transcript Alleles

HGVS Amino-acid change
ENST00000711046.1:c.60_61del ENSP00000518556.1:p.Leu21IlefsTer2
ENST00000437951.6:c.255_256del MANE Plus Clinical ENSP00000389744.2:p.Leu86IlefsTer2
ENST00000331920.11:c.258_259del MANE Select ENSP00000332353.6:p.Leu87IlefsTer2
ENST00000331920.10:c.258_259del ENSP00000332353.6:p.Leu87IlefsTer2
ENST00000375274.6:c.255_256del ENSP00000364423.2:p.Leu86IlefsTer2
ENST00000375290.6:c.57_58del ENSP00000364439.2:p.Leu20IlefsTer2
ENST00000418258.5:c.-196_-195del ENSP00000396135.1:n.-196_-195del
ENST00000421141.5:c.-196_-195del ENSP00000399981.1:n.-196_-195del
ENST00000429896.6:c.-196_-195del ENSP00000414823.2:n.-196_-195del
ENST00000430669.6:c.60_61del ENSP00000410287.2:p.Leu21IlefsTer2
ENST00000437951.5:c.60_61del ENSP00000389744.1:p.Leu21IlefsTer2
ENST00000468211.6:c.60_61del ENSP00000449745.1:p.Leu21IlefsTer2
ENST00000546820.5:c.-196_-195del ENSP00000448843.1:n.-196_-195del
ENST00000547672.5:c.-196_-195del ENSP00000447878.1:n.-196_-195del
ENST00000548420.1:c.-231_-230del ENSP00000449078.1:n.-231_-230del
ENST00000548945.6:n.57_58del
ENST00000550914.6:c.-196_-195del ENSP00000450047.1:n.-196_-195del
ENST00000551425.1:n.190+9926_190+9927del
ENST00000551623.1:c.36+10080_36+10081del ENSP00000447242.1:n.36+10080_36+10081del
ENST00000551630.1:c.-196_-195del ENSP00000450131.1:n.-196_-195del
ENST00000551845.5:c.-196_-195del ENSP00000447008.1:n.-196_-195del
ENST00000553011.5:c.-196_-195del ENSP00000447797.1:n.-196_-195del
NM_000264.3:c.258_259del , LRG_515t1:c.258_259del NP_000255.2:p.Leu87IlefsTer2
NM_001083602.1:c.60_61del , LRG_515t2:c.60_61del NP_001077071.1:p.Leu21IlefsTer2
NM_001083603.1:c.255_256del NP_001077072.1:p.Leu86IlefsTer2
NM_001083604.1:c.-196_-195del NP_001077073.1:n.-196_-195del
NM_001083605.1:c.-196_-195del NP_001077074.1:n.-196_-195del
NM_001083606.1:c.-196_-195del NP_001077075.1:n.-196_-195del
NM_001083607.1:c.-196_-195del NP_001077076.1:n.-196_-195del
XM_011518868.1:c.258_259del XP_011517170.1:p.Leu87IlefsTer2
XM_011518871.1:c.-60+9926_-60+9927del XP_011517173.1:n.-60+9926_-60+9927del
XM_011518873.1:c.-231_-230del XP_011517175.1:n.-231_-230del
XM_011518874.1:c.258_259del XP_011517176.1:p.Leu87IlefsTer2
NM_000264.4:c.258_259del NP_000255.2:p.Leu87IlefsTer2
NM_001083602.2:c.60_61del NP_001077071.1:p.Leu21IlefsTer2
NM_001083603.2:c.255_256del NP_001077072.1:p.Leu86IlefsTer2
NM_001083604.2:c.-196_-195del NP_001077073.1:n.-196_-195del
NM_001083605.2:c.-196_-195del NP_001077074.1:n.-196_-195del
NM_001083606.2:c.-196_-195del NP_001077075.1:n.-196_-195del
NM_001083607.2:c.-196_-195del NP_001077076.1:n.-196_-195del
NM_001354918.1:c.258_259del NP_001341847.1:p.Leu87IlefsTer2
NM_001354919.1:c.60_61del NP_001341848.1:p.Leu21IlefsTer2
NR_149061.1:n.446_447del
NM_000264.5:c.258_259del MANE Select NP_000255.2:p.Leu87IlefsTer2
NM_001083606.3:c.-196_-195del NP_001077075.1:n.-196_-195del
NM_001354918.2:c.258_259del NP_001341847.1:p.Leu87IlefsTer2
NR_149061.2:n.1163_1164del
NM_001083602.3:c.60_61del NP_001077071.1:p.Leu21IlefsTer2
NM_001083603.3:c.255_256del MANE Plus Clinical NP_001077072.1:p.Leu86IlefsTer2
NM_001083604.3:c.-196_-195del NP_001077073.1:n.-196_-195del
NM_001083605.3:c.-196_-195del NP_001077074.1:n.-196_-195del
NM_001083607.3:c.-196_-195del NP_001077076.1:n.-196_-195del
NM_001354919.2:c.60_61del NP_001341848.1:p.Leu21IlefsTer2