Canonical Allele Identifier: CA1865612422
Gene: PTCH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95482160_95482161delinsTA , CM000671.2:g.95482160_95482161delinsTA GRCh38
NC_000009.11:g.98244442_98244443delinsTA , CM000671.1:g.98244442_98244443delinsTA GRCh37
NC_000009.10:g.97284263_97284264delinsTA NCBI36
NG_007664.1:g.39805_39806delinsTA , LRG_515:g.39805_39806delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000711046.1:c.429_430delinsTA ENSP00000518556.1:p.Leu143=
ENST00000437951.6:c.624_625delinsTA MANE Plus Clinical ENSP00000389744.2:p.Leu208=
ENST00000690194.1:c.174_175delinsTA ENSP00000509379.1:p.Leu58=
ENST00000692981.1:c.174_175delinsTA ENSP00000510238.1:p.Leu58=
ENST00000331920.11:c.627_628delinsTA MANE Select ENSP00000332353.6:p.Leu209=
ENST00000331920.10:c.627_628delinsTA ENSP00000332353.6:p.Leu209=
ENST00000375274.6:c.624_625delinsTA ENSP00000364423.2:p.Leu208=
ENST00000375290.6:c.384-1573_384-1572delinsTA ENSP00000364439.2:n.384-1573_384-1572delinsTA
ENST00000418258.5:c.174_175delinsTA ENSP00000396135.1:p.Leu58=
ENST00000421141.5:c.174_175delinsTA ENSP00000399981.1:p.Leu58=
ENST00000429896.6:c.174_175delinsTA ENSP00000414823.2:p.Leu58=
ENST00000430669.6:c.429_430delinsTA ENSP00000410287.2:p.Leu143=
ENST00000437951.5:c.429_430delinsTA ENSP00000389744.1:p.Leu143=
ENST00000468211.6:c.429_430delinsTA ENSP00000449745.1:p.Leu143=
ENST00000546820.5:c.174_175delinsTA ENSP00000448843.1:p.Leu58=
ENST00000547672.5:c.174_175delinsTA ENSP00000447878.1:p.Leu58=
ENST00000548379.5:n.280_281delinsTA
ENST00000548420.1:c.-94-1573_-94-1572delinsTA ENSP00000449078.1:n.-94-1573_-94-1572delinsTA
ENST00000548945.6:n.194-1573_194-1572delinsTA
ENST00000550136.1:n.2149_2150delinsTA
ENST00000550914.6:c.209_210delinsTA ENSP00000450047.1:p.Leu70=
ENST00000551623.1:c.269_270delinsTA ENSP00000447242.1:n.269_270delinsTA
ENST00000551630.1:c.174_175delinsTA ENSP00000450131.1:p.Leu58=
ENST00000551845.5:c.174_175delinsTA ENSP00000447008.1:p.Leu58=
ENST00000553011.5:c.174_175delinsTA ENSP00000447797.1:p.Leu58=
ENST00000553256.5:n.373_374delinsTA
NM_000264.3:c.627_628delinsTA , LRG_515t1:c.627_628delinsTA NP_000255.2:p.Leu209=
NM_001083602.1:c.429_430delinsTA , LRG_515t2:c.429_430delinsTA NP_001077071.1:p.Leu143=
NM_001083603.1:c.624_625delinsTA NP_001077072.1:p.Leu208=
NM_001083604.1:c.174_175delinsTA NP_001077073.1:p.Leu58=
NM_001083605.1:c.174_175delinsTA NP_001077074.1:p.Leu58=
NM_001083606.1:c.174_175delinsTA NP_001077075.1:p.Leu58=
NM_001083607.1:c.174_175delinsTA NP_001077076.1:p.Leu58=
XM_005252102.2:c.174_175delinsTA XP_005252159.1:p.Leu58=
XM_011518868.1:c.627_628delinsTA XP_011517170.1:p.Leu209=
XM_011518869.1:c.174_175delinsTA XP_011517171.1:p.Leu58=
XM_011518870.1:c.174_175delinsTA XP_011517172.1:p.Leu58=
XM_011518871.1:c.174_175delinsTA XP_011517173.1:p.Leu58=
XM_011518872.1:c.174_175delinsTA XP_011517174.1:p.Leu58=
XM_011518873.1:c.-94-1573_-94-1572delinsTA XP_011517175.1:n.-94-1573_-94-1572delinsTA
XM_011518874.1:c.627_628delinsTA XP_011517176.1:p.Leu209=
NM_000264.4:c.627_628delinsTA NP_000255.2:p.Leu209=
NM_001083602.2:c.429_430delinsTA NP_001077071.1:p.Leu143=
NM_001083603.2:c.624_625delinsTA NP_001077072.1:p.Leu208=
NM_001083604.2:c.174_175delinsTA NP_001077073.1:p.Leu58=
NM_001083605.2:c.174_175delinsTA NP_001077074.1:p.Leu58=
NM_001083606.2:c.174_175delinsTA NP_001077075.1:p.Leu58=
NM_001083607.2:c.174_175delinsTA NP_001077076.1:p.Leu58=
NM_001354918.1:c.627_628delinsTA NP_001341847.1:p.Leu209=
NM_001354919.1:c.429_430delinsTA NP_001341848.1:p.Leu143=
NR_149061.1:n.815_816delinsTA
NM_000264.5:c.627_628delinsTA MANE Select NP_000255.2:p.Leu209=
NM_001083606.3:c.174_175delinsTA NP_001077075.1:p.Leu58=
NM_001354918.2:c.627_628delinsTA NP_001341847.1:p.Leu209=
NR_149061.2:n.1532_1533delinsTA
NM_001083602.3:c.429_430delinsTA NP_001077071.1:p.Leu143=
NM_001083603.3:c.624_625delinsTA MANE Plus Clinical NP_001077072.1:p.Leu208=
NM_001083604.3:c.174_175delinsTA NP_001077073.1:p.Leu58=
NM_001083605.3:c.174_175delinsTA NP_001077074.1:p.Leu58=
NM_001083607.3:c.174_175delinsTA NP_001077076.1:p.Leu58=
NM_001354919.2:c.429_430delinsTA NP_001341848.1:p.Leu143=