Canonical Allele Identifier: CA337851

Gene: PTCH1

Linked Data

• ClinVar Variation Id: 216369
• ClinVar RCV Id: RCV000198359
• dbSNP Id: rs768956985
• ExAC: 9:98240410 G / A
• gnomAD v2: 9-98240410-G-A
• gnomAD v4: 9-95478128-G-A
• COSMIC: COSM3780225 ; COSM3780226 ; COSM3780227 ; COSM3780228
• MyVariant Identifiers: chr9:g.98240410G>A (hg19) ; chr9:g.95478128G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95478128G>A , CM000671.2:g.95478128G>A	GRCh38
NC_000009.11:g.98240410G>A , CM000671.1:g.98240410G>A	GRCh37
NC_000009.10:g.97280231G>A	NCBI36
NG_007664.1:g.43838C>T , LRG_515:g.43838C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000711046.1:c.1076C>T	ENSP00000518556.1:p.Thr359Met
ENST00000437951.6:c.1271C>T MANE Plus Clinical	ENSP00000389744.2:p.Thr424Met
ENST00000690194.1:c.821C>T	ENSP00000509379.1:p.Thr274Met
ENST00000692981.1:c.821C>T	ENSP00000510238.1:p.Thr274Met
ENST00000331920.11:c.1274C>T MANE Select	ENSP00000332353.6:p.Thr425Met
ENST00000331920.10:c.1274C>T	ENSP00000332353.6:p.Thr425Met
ENST00000375271.4:c.425C>T	ENSP00000364420.4:p.Thr142Met
ENST00000375274.6:c.1271C>T	ENSP00000364423.2:p.Thr424Met
ENST00000375290.6:c.911C>T	ENSP00000364439.2:p.Thr304Met
ENST00000418258.5:c.821C>T	ENSP00000396135.1:p.Thr274Met
ENST00000421141.5:c.821C>T	ENSP00000399981.1:p.Thr274Met
ENST00000429896.6:c.821C>T	ENSP00000414823.2:p.Thr274Met
ENST00000430669.6:c.1076C>T	ENSP00000410287.2:p.Thr359Met
ENST00000437951.5:c.1076C>T	ENSP00000389744.1:p.Thr359Met
NM_000264.3:c.1274C>T , LRG_515t1:c.1274C>T	NP_000255.2:p.Thr425Met
NM_001083602.1:c.1076C>T , LRG_515t2:c.1076C>T	NP_001077071.1:p.Thr359Met
NM_001083603.1:c.1271C>T	NP_001077072.1:p.Thr424Met
NM_001083604.1:c.821C>T	NP_001077073.1:p.Thr274Met
NM_001083605.1:c.821C>T	NP_001077074.1:p.Thr274Met
NM_001083606.1:c.821C>T	NP_001077075.1:p.Thr274Met
NM_001083607.1:c.821C>T	NP_001077076.1:p.Thr274Met
XM_005252102.2:c.821C>T	XP_005252159.1:p.Thr274Met
XM_011518868.1:c.1274C>T	XP_011517170.1:p.Thr425Met
XM_011518869.1:c.821C>T	XP_011517171.1:p.Thr274Met
XM_011518870.1:c.821C>T	XP_011517172.1:p.Thr274Met
XM_011518871.1:c.821C>T	XP_011517173.1:p.Thr274Met
XM_011518872.1:c.821C>T	XP_011517174.1:p.Thr274Met
XM_011518873.1:c.434C>T	XP_011517175.1:p.Thr145Met
XM_011518874.1:c.1274C>T	XP_011517176.1:p.Thr425Met
NM_000264.4:c.1274C>T	NP_000255.2:p.Thr425Met
NM_001083602.2:c.1076C>T	NP_001077071.1:p.Thr359Met
NM_001083603.2:c.1271C>T	NP_001077072.1:p.Thr424Met
NM_001083604.2:c.821C>T	NP_001077073.1:p.Thr274Met
NM_001083605.2:c.821C>T	NP_001077074.1:p.Thr274Met
NM_001083606.2:c.821C>T	NP_001077075.1:p.Thr274Met
NM_001083607.2:c.821C>T	NP_001077076.1:p.Thr274Met
NM_001354918.1:c.1274C>T	NP_001341847.1:p.Thr425Met
NR_149061.1:n.1462C>T
NM_000264.5:c.1274C>T MANE Select	NP_000255.2:p.Thr425Met
NM_001083606.3:c.821C>T	NP_001077075.1:p.Thr274Met
NM_001354918.2:c.1274C>T	NP_001341847.1:p.Thr425Met
NR_149061.2:n.2179C>T
NM_001083602.3:c.1076C>T	NP_001077071.1:p.Thr359Met
NM_001083603.3:c.1271C>T MANE Plus Clinical	NP_001077072.1:p.Thr424Met
NM_001083604.3:c.821C>T	NP_001077073.1:p.Thr274Met
NM_001083605.3:c.821C>T	NP_001077074.1:p.Thr274Met
NM_001083607.3:c.821C>T	NP_001077076.1:p.Thr274Met