Canonical Allele Identifier: CA10634162

Gene: PTCH1

Linked Data

• ClinVar Variation Id: 367619
• ClinVar RCV Id: RCV000351583 ; RCV000389846
• dbSNP Id: rs992312438
• gnomAD v4: 9-95443180-A-G
• MyVariant Identifiers: chr9:g.98205462A>G (hg19) ; chr9:g.95443180A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95443180A>G , CM000671.2:g.95443180A>G	GRCh38
NC_000009.11:g.98205462A>G , CM000671.1:g.98205462A>G	GRCh37
NC_000009.10:g.97245283A>G	NCBI36
NG_007664.1:g.78786T>C , LRG_515:g.78786T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711046.1:c.*3213T>C	ENSP00000518556.1:n.*3213T>C
ENST00000437951.6:c.*3213T>C MANE Plus Clinical	ENSP00000389744.2:n.*3213T>C
ENST00000331920.11:c.*3213T>C MANE Select	ENSP00000332353.6:n.*3213T>C
ENST00000331920.10:c.*3213T>C	ENSP00000332353.6:n.*3213T>C
ENST00000418258.5:c.*3213T>C	ENSP00000396135.1:n.*3213T>C
ENST00000421141.5:c.*3213T>C	ENSP00000399981.1:n.*3213T>C
ENST00000437951.5:c.*3213T>C	ENSP00000389744.1:n.*3213T>C
NM_000264.3:c.*3213T>C , LRG_515t1:c.*3213T>C	NP_000255.2:n.*3213T>C
NM_001083602.1:c.*3213T>C , LRG_515t2:c.*3213T>C	NP_001077071.1:n.*3213T>C
NM_001083603.1:c.*3213T>C	NP_001077072.1:n.*3213T>C
NM_001083604.1:c.*3213T>C	NP_001077073.1:n.*3213T>C
NM_001083605.1:c.*3213T>C	NP_001077074.1:n.*3213T>C
NM_001083606.1:c.*3213T>C	NP_001077075.1:n.*3213T>C
NM_001083607.1:c.*3213T>C	NP_001077076.1:n.*3213T>C
XM_005252102.2:c.*3213T>C	XP_005252159.1:n.*3213T>C
XM_011518868.1:c.*3213T>C	XP_011517170.1:n.*3213T>C
XM_011518869.1:c.*3213T>C	XP_011517171.1:n.*3213T>C
XM_011518870.1:c.*3213T>C	XP_011517172.1:n.*3213T>C
XM_011518871.1:c.*3213T>C	XP_011517173.1:n.*3213T>C
XM_011518872.1:c.*3213T>C	XP_011517174.1:n.*3213T>C
XM_011518873.1:c.*3213T>C	XP_011517175.1:n.*3213T>C
NM_000264.4:c.*3213T>C	NP_000255.2:n.*3213T>C
NM_001083602.2:c.*3213T>C	NP_001077071.1:n.*3213T>C
NM_001083603.2:c.*3213T>C	NP_001077072.1:n.*3213T>C
NM_001083604.2:c.*3213T>C	NP_001077073.1:n.*3213T>C
NM_001083605.2:c.*3213T>C	NP_001077074.1:n.*3213T>C
NM_001083606.2:c.*3213T>C	NP_001077075.1:n.*3213T>C
NM_001083607.2:c.*3213T>C	NP_001077076.1:n.*3213T>C
NM_001354918.1:c.*3213T>C	NP_001341847.1:n.*3213T>C
NR_149061.1:n.7579T>C
NM_000264.5:c.*3213T>C MANE Select	NP_000255.2:n.*3213T>C
NM_001083606.3:c.*3213T>C	NP_001077075.1:n.*3213T>C
NM_001354918.2:c.*3213T>C	NP_001341847.1:n.*3213T>C
NR_149061.2:n.8296T>C
NM_001083602.3:c.*3213T>C	NP_001077071.1:n.*3213T>C
NM_001083603.3:c.*3213T>C MANE Plus Clinical	NP_001077072.1:n.*3213T>C
NM_001083604.3:c.*3213T>C	NP_001077073.1:n.*3213T>C
NM_001083605.3:c.*3213T>C	NP_001077074.1:n.*3213T>C
NM_001083607.3:c.*3213T>C	NP_001077076.1:n.*3213T>C