Canonical Allele Identifier: CA1865583896

Gene: PTCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95453542_95453543delinsCA , CM000671.2:g.95453542_95453543delinsCA	GRCh38
NC_000009.11:g.98215824_98215825delinsCA , CM000671.1:g.98215824_98215825delinsCA	GRCh37
NC_000009.10:g.97255645_97255646delinsCA	NCBI36
NG_007664.1:g.68423_68424delinsTG , LRG_515:g.68423_68424delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711046.1:c.3186_3187delinsTG	ENSP00000518556.1:p.Asp1062=
ENST00000437951.6:c.3381_3382delinsTG MANE Plus Clinical	ENSP00000389744.2:p.Asp1127=
ENST00000690194.1:c.*1692_*1693delinsTG	ENSP00000509379.1:n.*1692_*1693delinsTG
ENST00000692981.1:c.2931_2932delinsTG	ENSP00000510238.1:p.Asp977=
ENST00000693534.1:n.715_716delinsTG
ENST00000331920.11:c.3384_3385delinsTG MANE Select	ENSP00000332353.6:p.Asp1128=
ENST00000331920.10:c.3384_3385delinsTG	ENSP00000332353.6:p.Asp1128=
ENST00000375274.6:c.3381_3382delinsTG	ENSP00000364423.2:p.Asp1127=
ENST00000375290.6:c.3153_3154delinsTG	ENSP00000364439.2:n.3153_3154delinsTG
ENST00000418258.5:c.2931_2932delinsTG	ENSP00000396135.1:p.Asp977=
ENST00000421141.5:c.2931_2932delinsTG	ENSP00000399981.1:p.Asp977=
ENST00000429896.6:c.2931_2932delinsTG	ENSP00000414823.2:p.Asp977=
ENST00000430669.6:c.3186_3187delinsTG	ENSP00000410287.2:p.Asp1062=
ENST00000437951.5:c.3186_3187delinsTG	ENSP00000389744.1:p.Asp1062=
NM_000264.3:c.3384_3385delinsTG , LRG_515t1:c.3384_3385delinsTG	NP_000255.2:p.Asp1128=
NM_001083602.1:c.3186_3187delinsTG , LRG_515t2:c.3186_3187delinsTG	NP_001077071.1:p.Asp1062=
NM_001083603.1:c.3381_3382delinsTG	NP_001077072.1:p.Asp1127=
NM_001083604.1:c.2931_2932delinsTG	NP_001077073.1:p.Asp977=
NM_001083605.1:c.2931_2932delinsTG	NP_001077074.1:p.Asp977=
NM_001083606.1:c.2931_2932delinsTG	NP_001077075.1:p.Asp977=
NM_001083607.1:c.2931_2932delinsTG	NP_001077076.1:p.Asp977=
XM_005252102.2:c.2931_2932delinsTG	XP_005252159.1:p.Asp977=
XM_011518868.1:c.3228_3229delinsTG	XP_011517170.1:p.Asp1076=
XM_011518869.1:c.2931_2932delinsTG	XP_011517171.1:p.Asp977=
XM_011518870.1:c.2931_2932delinsTG	XP_011517172.1:p.Asp977=
XM_011518871.1:c.2931_2932delinsTG	XP_011517173.1:p.Asp977=
XM_011518872.1:c.2931_2932delinsTG	XP_011517174.1:p.Asp977=
XM_011518873.1:c.2544_2545delinsTG	XP_011517175.1:p.Asp848=
XM_011518874.1:c.3384_3385delinsTG	XP_011517176.1:p.Asp1128=
NM_000264.4:c.3384_3385delinsTG	NP_000255.2:p.Asp1128=
NM_001083602.2:c.3186_3187delinsTG	NP_001077071.1:p.Asp1062=
NM_001083603.2:c.3381_3382delinsTG	NP_001077072.1:p.Asp1127=
NM_001083604.2:c.2931_2932delinsTG	NP_001077073.1:p.Asp977=
NM_001083605.2:c.2931_2932delinsTG	NP_001077074.1:p.Asp977=
NM_001083606.2:c.2931_2932delinsTG	NP_001077075.1:p.Asp977=
NM_001083607.2:c.2931_2932delinsTG	NP_001077076.1:p.Asp977=
NM_001354918.1:c.3228_3229delinsTG	NP_001341847.1:p.Asp1076=
NR_149061.1:n.3406_3407delinsTG
NM_000264.5:c.3384_3385delinsTG MANE Select	NP_000255.2:p.Asp1128=
NM_001083606.3:c.2931_2932delinsTG	NP_001077075.1:p.Asp977=
NM_001354918.2:c.3228_3229delinsTG	NP_001341847.1:p.Asp1076=
NR_149061.2:n.4123_4124delinsTG
NM_001083602.3:c.3186_3187delinsTG	NP_001077071.1:p.Asp1062=
NM_001083603.3:c.3381_3382delinsTG MANE Plus Clinical	NP_001077072.1:p.Asp1127=
NM_001083604.3:c.2931_2932delinsTG	NP_001077073.1:p.Asp977=
NM_001083605.3:c.2931_2932delinsTG	NP_001077074.1:p.Asp977=
NM_001083607.3:c.2931_2932delinsTG	NP_001077076.1:p.Asp977=