Canonical Allele Identifier: CA10634198

Gene: PTCH1

Linked Data

• ClinVar Variation Id: 367646
• ClinVar RCV Id: RCV000317879 ; RCV000353980 ; RCV001692082
• dbSNP Id: rs16909865
• gnomAD v2: 9-98207302-C-G
• gnomAD v3: 9-95445020-C-G
• gnomAD v4: 9-95445020-C-G
• MyVariant Identifiers: chr9:g.98207302C>G (hg19) ; chr9:g.95445020C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95445020C>G , CM000671.2:g.95445020C>G	GRCh38
NC_000009.11:g.98207302C>G , CM000671.1:g.98207302C>G	GRCh37
NC_000009.10:g.97247123C>G	NCBI36
NG_007664.1:g.76946G>C , LRG_515:g.76946G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711046.1:c.*1373G>C	ENSP00000518556.1:n.*1373G>C
ENST00000437951.6:c.*1373G>C MANE Plus Clinical	ENSP00000389744.2:n.*1373G>C
ENST00000687744.1:n.4433G>C
ENST00000690194.1:c.*4025G>C	ENSP00000509379.1:n.*4025G>C
ENST00000692981.1:c.*1373G>C	ENSP00000510238.1:n.*1373G>C
ENST00000693534.1:n.3064G>C
ENST00000331920.11:c.*1373G>C MANE Select	ENSP00000332353.6:n.*1373G>C
ENST00000331920.10:c.*1373G>C	ENSP00000332353.6:n.*1373G>C
ENST00000375290.6:c.9023G>C	ENSP00000364439.2:n.9023G>C
ENST00000418258.5:c.*1373G>C	ENSP00000396135.1:n.*1373G>C
ENST00000421141.5:c.*1373G>C	ENSP00000399981.1:n.*1373G>C
ENST00000429896.6:c.*1373G>C	ENSP00000414823.2:n.*1373G>C
ENST00000430669.6:c.*1892G>C	ENSP00000410287.2:n.*1892G>C
ENST00000437951.5:c.*1373G>C	ENSP00000389744.1:n.*1373G>C
ENST00000546744.5:n.2781G>C
NM_000264.3:c.*1373G>C , LRG_515t1:c.*1373G>C	NP_000255.2:n.*1373G>C
NM_001083602.1:c.*1373G>C , LRG_515t2:c.*1373G>C	NP_001077071.1:n.*1373G>C
NM_001083603.1:c.*1373G>C	NP_001077072.1:n.*1373G>C
NM_001083604.1:c.*1373G>C	NP_001077073.1:n.*1373G>C
NM_001083605.1:c.*1373G>C	NP_001077074.1:n.*1373G>C
NM_001083606.1:c.*1373G>C	NP_001077075.1:n.*1373G>C
NM_001083607.1:c.*1373G>C	NP_001077076.1:n.*1373G>C
XM_005252102.2:c.*1373G>C	XP_005252159.1:n.*1373G>C
XM_011518868.1:c.*1373G>C	XP_011517170.1:n.*1373G>C
XM_011518869.1:c.*1373G>C	XP_011517171.1:n.*1373G>C
XM_011518870.1:c.*1373G>C	XP_011517172.1:n.*1373G>C
XM_011518871.1:c.*1373G>C	XP_011517173.1:n.*1373G>C
XM_011518872.1:c.*1373G>C	XP_011517174.1:n.*1373G>C
XM_011518873.1:c.*1373G>C	XP_011517175.1:n.*1373G>C
NM_000264.4:c.*1373G>C	NP_000255.2:n.*1373G>C
NM_001083602.2:c.*1373G>C	NP_001077071.1:n.*1373G>C
NM_001083603.2:c.*1373G>C	NP_001077072.1:n.*1373G>C
NM_001083604.2:c.*1373G>C	NP_001077073.1:n.*1373G>C
NM_001083605.2:c.*1373G>C	NP_001077074.1:n.*1373G>C
NM_001083606.2:c.*1373G>C	NP_001077075.1:n.*1373G>C
NM_001083607.2:c.*1373G>C	NP_001077076.1:n.*1373G>C
NM_001354918.1:c.*1373G>C	NP_001341847.1:n.*1373G>C
NR_149061.1:n.5739G>C
NM_000264.5:c.*1373G>C MANE Select	NP_000255.2:n.*1373G>C
NM_001083606.3:c.*1373G>C	NP_001077075.1:n.*1373G>C
NM_001354918.2:c.*1373G>C	NP_001341847.1:n.*1373G>C
NR_149061.2:n.6456G>C
NM_001083602.3:c.*1373G>C	NP_001077071.1:n.*1373G>C
NM_001083603.3:c.*1373G>C MANE Plus Clinical	NP_001077072.1:n.*1373G>C
NM_001083604.3:c.*1373G>C	NP_001077073.1:n.*1373G>C
NM_001083605.3:c.*1373G>C	NP_001077074.1:n.*1373G>C
NM_001083607.3:c.*1373G>C	NP_001077076.1:n.*1373G>C