Canonical Allele Identifier: CA350057
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 220567
ClinVar RCV Id: RCV000205973
dbSNP Id: rs864622583

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95506499_95506533del , CM000671.2:g.95506499_95506533del GRCh38
NC_000009.11:g.98268781_98268815del , CM000671.1:g.98268781_98268815del GRCh37
NC_000009.10:g.97308602_97308636del NCBI36
NG_007664.1:g.15435_15469del , LRG_515:g.15435_15469del

Transcript Alleles

HGVS Amino-acid change
ENST00000711046.1:c.72_106del ENSP00000518556.1:p.Tyr27GlyfsTer?
ENST00000437951.6:c.267_301del MANE Plus Clinical ENSP00000389744.2:p.Tyr92GlyfsTer?
ENST00000331920.11:c.270_304del MANE Select ENSP00000332353.6:p.Tyr93GlyfsTer?
ENST00000331920.10:c.270_304del ENSP00000332353.6:p.Tyr93GlyfsTer?
ENST00000375274.6:c.267_301del ENSP00000364423.2:p.Tyr92GlyfsTer?
ENST00000375290.6:c.69_103del ENSP00000364439.2:p.Tyr26GlyfsTer?
ENST00000418258.5:c.-184_-150del ENSP00000396135.1:n.-184_-150del
ENST00000421141.5:c.-184_-150del ENSP00000399981.1:n.-184_-150del
ENST00000429896.6:c.-184_-150del ENSP00000414823.2:n.-184_-150del
ENST00000430669.6:c.72_106del ENSP00000410287.2:p.Tyr27GlyfsTer?
ENST00000437951.5:c.72_106del ENSP00000389744.1:p.Tyr27GlyfsTer?
ENST00000468211.6:c.72_106del ENSP00000449745.1:p.Tyr27GlyfsTer?
ENST00000546820.5:c.-184_-150del ENSP00000448843.1:n.-184_-150del
ENST00000547672.5:c.-184_-150del ENSP00000447878.1:n.-184_-150del
ENST00000548420.1:c.-219_-185del ENSP00000449078.1:n.-219_-185del
ENST00000548945.6:n.69_103del
ENST00000550914.6:c.-184_-150del ENSP00000450047.1:n.-184_-150del
ENST00000551425.1:n.190+9938_190+9972del
ENST00000551623.1:c.36+10092_36+10126del ENSP00000447242.1:n.36+10092_36+10126del
ENST00000551630.1:c.-184_-150del ENSP00000450131.1:n.-184_-150del
ENST00000551845.5:c.-184_-150del ENSP00000447008.1:n.-184_-150del
ENST00000553011.5:c.-184_-150del ENSP00000447797.1:n.-184_-150del
NM_000264.3:c.270_304del , LRG_515t1:c.270_304del NP_000255.2:p.Tyr93GlyfsTer?
NM_001083602.1:c.72_106del , LRG_515t2:c.72_106del NP_001077071.1:p.Tyr27GlyfsTer?
NM_001083603.1:c.267_301del NP_001077072.1:p.Tyr92GlyfsTer?
NM_001083604.1:c.-184_-150del NP_001077073.1:n.-184_-150del
NM_001083605.1:c.-184_-150del NP_001077074.1:n.-184_-150del
NM_001083606.1:c.-184_-150del NP_001077075.1:n.-184_-150del
NM_001083607.1:c.-184_-150del NP_001077076.1:n.-184_-150del
XM_011518868.1:c.270_304del XP_011517170.1:p.Tyr93GlyfsTer?
XM_011518871.1:c.-60+9938_-60+9972del XP_011517173.1:n.-60+9938_-60+9972del
XM_011518873.1:c.-219_-185del XP_011517175.1:n.-219_-185del
XM_011518874.1:c.270_304del XP_011517176.1:p.Tyr93GlyfsTer?
NM_000264.4:c.270_304del NP_000255.2:p.Tyr93GlyfsTer?
NM_001083602.2:c.72_106del NP_001077071.1:p.Tyr27GlyfsTer?
NM_001083603.2:c.267_301del NP_001077072.1:p.Tyr92GlyfsTer?
NM_001083604.2:c.-184_-150del NP_001077073.1:n.-184_-150del
NM_001083605.2:c.-184_-150del NP_001077074.1:n.-184_-150del
NM_001083606.2:c.-184_-150del NP_001077075.1:n.-184_-150del
NM_001083607.2:c.-184_-150del NP_001077076.1:n.-184_-150del
NM_001354918.1:c.270_304del NP_001341847.1:p.Tyr93GlyfsTer?
NM_001354919.1:c.72_106del NP_001341848.1:p.Tyr27GlyfsTer?
NR_149061.1:n.458_492del
NM_000264.5:c.270_304del MANE Select NP_000255.2:p.Tyr93GlyfsTer?
NM_001083606.3:c.-184_-150del NP_001077075.1:n.-184_-150del
NM_001354918.2:c.270_304del NP_001341847.1:p.Tyr93GlyfsTer?
NR_149061.2:n.1175_1209del
NM_001083602.3:c.72_106del NP_001077071.1:p.Tyr27GlyfsTer?
NM_001083603.3:c.267_301del MANE Plus Clinical NP_001077072.1:p.Tyr92GlyfsTer?
NM_001083604.3:c.-184_-150del NP_001077073.1:n.-184_-150del
NM_001083605.3:c.-184_-150del NP_001077074.1:n.-184_-150del
NM_001083607.3:c.-184_-150del NP_001077076.1:n.-184_-150del
NM_001354919.2:c.72_106del NP_001341848.1:p.Tyr27GlyfsTer?