Canonical Allele Identifier: CA374111656

Gene: PTCH1

Linked Data

• ClinVar Variation Id: 1448301
• ClinVar RCV Id: RCV001997095 ; RCV002458871
• dbSNP Id: rs1439411173
• gnomAD v4: 9-95453483-A-C
• MyVariant Identifiers: chr9:g.98215765A>C (hg19) ; chr9:g.95453483A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95453483A>C , CM000671.2:g.95453483A>C	GRCh38
NC_000009.11:g.98215765A>C , CM000671.1:g.98215765A>C	GRCh37
NC_000009.10:g.97255586A>C	NCBI36
NG_007664.1:g.68483T>G , LRG_515:g.68483T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711046.1:c.3246T>G	ENSP00000518556.1:p.Ile1082Met
ENST00000437951.6:c.3441T>G MANE Plus Clinical	ENSP00000389744.2:p.Ile1147Met
ENST00000690194.1:c.*1752T>G	ENSP00000509379.1:n.*1752T>G
ENST00000692981.1:c.2991T>G	ENSP00000510238.1:p.Ile997Met
ENST00000693534.1:n.775T>G
ENST00000331920.11:c.3444T>G MANE Select	ENSP00000332353.6:p.Ile1148Met
ENST00000331920.10:c.3444T>G	ENSP00000332353.6:p.Ile1148Met
ENST00000375274.6:c.3441T>G	ENSP00000364423.2:p.Ile1147Met
ENST00000375290.6:c.3213T>G	ENSP00000364439.2:n.3213T>G
ENST00000418258.5:c.2991T>G	ENSP00000396135.1:p.Ile997Met
ENST00000421141.5:c.2991T>G	ENSP00000399981.1:p.Ile997Met
ENST00000429896.6:c.2991T>G	ENSP00000414823.2:p.Ile997Met
ENST00000430669.6:c.3246T>G	ENSP00000410287.2:p.Ile1082Met
ENST00000437951.5:c.3246T>G	ENSP00000389744.1:p.Ile1082Met
NM_000264.3:c.3444T>G , LRG_515t1:c.3444T>G	NP_000255.2:p.Ile1148Met
NM_001083602.1:c.3246T>G , LRG_515t2:c.3246T>G	NP_001077071.1:p.Ile1082Met
NM_001083603.1:c.3441T>G	NP_001077072.1:p.Ile1147Met
NM_001083604.1:c.2991T>G	NP_001077073.1:p.Ile997Met
NM_001083605.1:c.2991T>G	NP_001077074.1:p.Ile997Met
NM_001083606.1:c.2991T>G	NP_001077075.1:p.Ile997Met
NM_001083607.1:c.2991T>G	NP_001077076.1:p.Ile997Met
XM_005252102.2:c.2991T>G	XP_005252159.1:p.Ile997Met
XM_011518868.1:c.3288T>G	XP_011517170.1:p.Ile1096Met
XM_011518869.1:c.2991T>G	XP_011517171.1:p.Ile997Met
XM_011518870.1:c.2991T>G	XP_011517172.1:p.Ile997Met
XM_011518871.1:c.2991T>G	XP_011517173.1:p.Ile997Met
XM_011518872.1:c.2991T>G	XP_011517174.1:p.Ile997Met
XM_011518873.1:c.2604T>G	XP_011517175.1:p.Ile868Met
XM_011518874.1:c.3444T>G	XP_011517176.1:p.Ile1148Met
NM_000264.4:c.3444T>G	NP_000255.2:p.Ile1148Met
NM_001083602.2:c.3246T>G	NP_001077071.1:p.Ile1082Met
NM_001083603.2:c.3441T>G	NP_001077072.1:p.Ile1147Met
NM_001083604.2:c.2991T>G	NP_001077073.1:p.Ile997Met
NM_001083605.2:c.2991T>G	NP_001077074.1:p.Ile997Met
NM_001083606.2:c.2991T>G	NP_001077075.1:p.Ile997Met
NM_001083607.2:c.2991T>G	NP_001077076.1:p.Ile997Met
NM_001354918.1:c.3288T>G	NP_001341847.1:p.Ile1096Met
NR_149061.1:n.3466T>G
NM_000264.5:c.3444T>G MANE Select	NP_000255.2:p.Ile1148Met
NM_001083606.3:c.2991T>G	NP_001077075.1:p.Ile997Met
NM_001354918.2:c.3288T>G	NP_001341847.1:p.Ile1096Met
NR_149061.2:n.4183T>G
NM_001083602.3:c.3246T>G	NP_001077071.1:p.Ile1082Met
NM_001083603.3:c.3441T>G MANE Plus Clinical	NP_001077072.1:p.Ile1147Met
NM_001083604.3:c.2991T>G	NP_001077073.1:p.Ile997Met
NM_001083605.3:c.2991T>G	NP_001077074.1:p.Ile997Met
NM_001083607.3:c.2991T>G	NP_001077076.1:p.Ile997Met