Canonical Allele Identifier: CA1865611869
Gene: PTCH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95481877A= , CM000671.2:g.95481877A= GRCh38
NC_000009.11:g.98244159A= , CM000671.1:g.98244159A= GRCh37
NC_000009.10:g.97283980A= NCBI36
NG_007664.1:g.40089T= , LRG_515:g.40089T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000711046.1:c.548+72T= ENSP00000518556.1:n.548+72T=
ENST00000437951.6:c.743+72T= MANE Plus Clinical ENSP00000389744.2:n.743+72T=
ENST00000690194.1:c.293+72T= ENSP00000509379.1:n.293+72T=
ENST00000692981.1:c.293+72T= ENSP00000510238.1:n.293+72T=
ENST00000331920.11:c.746+72T= MANE Select ENSP00000332353.6:n.746+72T=
ENST00000331920.10:c.746+72T= ENSP00000332353.6:n.746+72T=
ENST00000375274.6:c.743+72T= ENSP00000364423.2:n.743+72T=
ENST00000375290.6:c.384-1289T= ENSP00000364439.2:n.384-1289T=
ENST00000418258.5:c.293+72T= ENSP00000396135.1:n.293+72T=
ENST00000421141.5:c.293+72T= ENSP00000399981.1:n.293+72T=
ENST00000429896.6:c.293+72T= ENSP00000414823.2:n.293+72T=
ENST00000430669.6:c.548+72T= ENSP00000410287.2:n.548+72T=
ENST00000437951.5:c.548+72T= ENSP00000389744.1:n.548+72T=
ENST00000468211.6:c.*68T= ENSP00000449745.1:n.*68T=
ENST00000546820.5:c.293+72T= ENSP00000448843.1:n.293+72T=
ENST00000547672.5:c.293+72T= ENSP00000447878.1:n.293+72T=
ENST00000548379.5:n.399+72T=
ENST00000548420.1:c.-94-1289T= ENSP00000449078.1:n.-94-1289T=
ENST00000548945.6:n.194-1289T=
ENST00000550136.1:n.2340T=
ENST00000550914.6:c.*88+72T= ENSP00000450047.1:n.*88+72T=
ENST00000551845.5:c.293+72T= ENSP00000447008.1:n.293+72T=
ENST00000553011.5:c.293+72T= ENSP00000447797.1:n.293+72T=
ENST00000553256.5:n.492+72T=
NM_000264.3:c.746+72T= , LRG_515t1:c.746+72T= NP_000255.2:n.746+72T=
NM_001083602.1:c.548+72T= , LRG_515t2:c.548+72T= NP_001077071.1:n.548+72T=
NM_001083603.1:c.743+72T= NP_001077072.1:n.743+72T=
NM_001083604.1:c.293+72T= NP_001077073.1:n.293+72T=
NM_001083605.1:c.293+72T= NP_001077074.1:n.293+72T=
NM_001083606.1:c.293+72T= NP_001077075.1:n.293+72T=
NM_001083607.1:c.293+72T= NP_001077076.1:n.293+72T=
XM_005252102.2:c.293+72T= XP_005252159.1:n.293+72T=
XM_011518868.1:c.746+72T= XP_011517170.1:n.746+72T=
XM_011518869.1:c.293+72T= XP_011517171.1:n.293+72T=
XM_011518870.1:c.293+72T= XP_011517172.1:n.293+72T=
XM_011518871.1:c.293+72T= XP_011517173.1:n.293+72T=
XM_011518872.1:c.293+72T= XP_011517174.1:n.293+72T=
XM_011518873.1:c.-94-1289T= XP_011517175.1:n.-94-1289T=
XM_011518874.1:c.746+72T= XP_011517176.1:n.746+72T=
NM_000264.4:c.746+72T= NP_000255.2:n.746+72T=
NM_001083602.2:c.548+72T= NP_001077071.1:n.548+72T=
NM_001083603.2:c.743+72T= NP_001077072.1:n.743+72T=
NM_001083604.2:c.293+72T= NP_001077073.1:n.293+72T=
NM_001083605.2:c.293+72T= NP_001077074.1:n.293+72T=
NM_001083606.2:c.293+72T= NP_001077075.1:n.293+72T=
NM_001083607.2:c.293+72T= NP_001077076.1:n.293+72T=
NM_001354918.1:c.746+72T= NP_001341847.1:n.746+72T=
NM_001354919.1:c.*68T= NP_001341848.1:n.*68T=
NR_149061.1:n.934+72T=
NM_000264.5:c.746+72T= MANE Select NP_000255.2:n.746+72T=
NM_001083606.3:c.293+72T= NP_001077075.1:n.293+72T=
NM_001354918.2:c.746+72T= NP_001341847.1:n.746+72T=
NR_149061.2:n.1651+72T=
NM_001083602.3:c.548+72T= NP_001077071.1:n.548+72T=
NM_001083603.3:c.743+72T= MANE Plus Clinical NP_001077072.1:n.743+72T=
NM_001083604.3:c.293+72T= NP_001077073.1:n.293+72T=
NM_001083605.3:c.293+72T= NP_001077074.1:n.293+72T=
NM_001083607.3:c.293+72T= NP_001077076.1:n.293+72T=
NM_001354919.2:c.*68T= NP_001341848.1:n.*68T=