Canonical Allele Identifier: CA1865583974

Gene: PTCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95453561_95453563delinsCAT , CM000671.2:g.95453561_95453563delinsCAT	GRCh38
NC_000009.11:g.98215843_98215845delinsCAT , CM000671.1:g.98215843_98215845delinsCAT	GRCh37
NC_000009.10:g.97255664_97255666delinsCAT	NCBI36
NG_007664.1:g.68403_68405delinsATG , LRG_515:g.68403_68405delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711046.1:c.3166_3168delinsATG	ENSP00000518556.1:p.Met1056=
ENST00000437951.6:c.3361_3363delinsATG MANE Plus Clinical	ENSP00000389744.2:p.Met1121=
ENST00000690194.1:c.*1672_*1674delinsATG	ENSP00000509379.1:n.*1672_*1674delinsATG
ENST00000692981.1:c.2911_2913delinsATG	ENSP00000510238.1:p.Met971=
ENST00000693534.1:n.695_697delinsATG
ENST00000331920.11:c.3364_3366delinsATG MANE Select	ENSP00000332353.6:p.Met1122=
ENST00000331920.10:c.3364_3366delinsATG	ENSP00000332353.6:p.Met1122=
ENST00000375274.6:c.3361_3363delinsATG	ENSP00000364423.2:p.Met1121=
ENST00000375290.6:c.3133_3135delinsATG	ENSP00000364439.2:n.3133_3135delinsATG
ENST00000418258.5:c.2911_2913delinsATG	ENSP00000396135.1:p.Met971=
ENST00000421141.5:c.2911_2913delinsATG	ENSP00000399981.1:p.Met971=
ENST00000429896.6:c.2911_2913delinsATG	ENSP00000414823.2:p.Met971=
ENST00000430669.6:c.3166_3168delinsATG	ENSP00000410287.2:p.Met1056=
ENST00000437951.5:c.3166_3168delinsATG	ENSP00000389744.1:p.Met1056=
NM_000264.3:c.3364_3366delinsATG , LRG_515t1:c.3364_3366delinsATG	NP_000255.2:p.Met1122=
NM_001083602.1:c.3166_3168delinsATG , LRG_515t2:c.3166_3168delinsATG	NP_001077071.1:p.Met1056=
NM_001083603.1:c.3361_3363delinsATG	NP_001077072.1:p.Met1121=
NM_001083604.1:c.2911_2913delinsATG	NP_001077073.1:p.Met971=
NM_001083605.1:c.2911_2913delinsATG	NP_001077074.1:p.Met971=
NM_001083606.1:c.2911_2913delinsATG	NP_001077075.1:p.Met971=
NM_001083607.1:c.2911_2913delinsATG	NP_001077076.1:p.Met971=
XM_005252102.2:c.2911_2913delinsATG	XP_005252159.1:p.Met971=
XM_011518868.1:c.3208_3210delinsATG	XP_011517170.1:p.Met1070=
XM_011518869.1:c.2911_2913delinsATG	XP_011517171.1:p.Met971=
XM_011518870.1:c.2911_2913delinsATG	XP_011517172.1:p.Met971=
XM_011518871.1:c.2911_2913delinsATG	XP_011517173.1:p.Met971=
XM_011518872.1:c.2911_2913delinsATG	XP_011517174.1:p.Met971=
XM_011518873.1:c.2524_2526delinsATG	XP_011517175.1:p.Met842=
XM_011518874.1:c.3364_3366delinsATG	XP_011517176.1:p.Met1122=
NM_000264.4:c.3364_3366delinsATG	NP_000255.2:p.Met1122=
NM_001083602.2:c.3166_3168delinsATG	NP_001077071.1:p.Met1056=
NM_001083603.2:c.3361_3363delinsATG	NP_001077072.1:p.Met1121=
NM_001083604.2:c.2911_2913delinsATG	NP_001077073.1:p.Met971=
NM_001083605.2:c.2911_2913delinsATG	NP_001077074.1:p.Met971=
NM_001083606.2:c.2911_2913delinsATG	NP_001077075.1:p.Met971=
NM_001083607.2:c.2911_2913delinsATG	NP_001077076.1:p.Met971=
NM_001354918.1:c.3208_3210delinsATG	NP_001341847.1:p.Met1070=
NR_149061.1:n.3386_3388delinsATG
NM_000264.5:c.3364_3366delinsATG MANE Select	NP_000255.2:p.Met1122=
NM_001083606.3:c.2911_2913delinsATG	NP_001077075.1:p.Met971=
NM_001354918.2:c.3208_3210delinsATG	NP_001341847.1:p.Met1070=
NR_149061.2:n.4103_4105delinsATG
NM_001083602.3:c.3166_3168delinsATG	NP_001077071.1:p.Met1056=
NM_001083603.3:c.3361_3363delinsATG MANE Plus Clinical	NP_001077072.1:p.Met1121=
NM_001083604.3:c.2911_2913delinsATG	NP_001077073.1:p.Met971=
NM_001083605.3:c.2911_2913delinsATG	NP_001077074.1:p.Met971=
NM_001083607.3:c.2911_2913delinsATG	NP_001077076.1:p.Met971=