Canonical Allele Identifier: CA374118141

Gene: PTCH1

Linked Data

• ClinVar Variation Id: 573636
• ClinVar RCV Id: RCV000695355
• dbSNP Id: rs1060502277
• COSMIC: COSM1222415 ; COSM1222416 ; COSM1222417 ; COSM1222418
• MyVariant Identifiers: chr9:g.98239040C>T (hg19) ; chr9:g.95476758C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95476758C>T , CM000671.2:g.95476758C>T	GRCh38
NC_000009.11:g.98239040C>T , CM000671.1:g.98239040C>T	GRCh37
NC_000009.10:g.97278861C>T	NCBI36
NG_007664.1:g.45208G>A , LRG_515:g.45208G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000711046.1:c.1404+1G>A	ENSP00000518556.1:n.1404+1G>A
ENST00000437951.6:c.1599+1G>A MANE Plus Clinical	ENSP00000389744.2:n.1599+1G>A
ENST00000690194.1:c.1149+1G>A	ENSP00000509379.1:n.1149+1G>A
ENST00000692981.1:c.1149+1G>A	ENSP00000510238.1:n.1149+1G>A
ENST00000331920.11:c.1602+1G>A MANE Select	ENSP00000332353.6:n.1602+1G>A
ENST00000331920.10:c.1602+1G>A	ENSP00000332353.6:n.1602+1G>A
ENST00000375271.4:c.597+1G>A	ENSP00000364420.4:n.597+1G>A
ENST00000375274.6:c.1599+1G>A	ENSP00000364423.2:n.1599+1G>A
ENST00000375290.6:c.1239+1G>A	ENSP00000364439.2:n.1239+1G>A
ENST00000418258.5:c.1149+1G>A	ENSP00000396135.1:n.1149+1G>A
ENST00000421141.5:c.1149+1G>A	ENSP00000399981.1:n.1149+1G>A
ENST00000429896.6:c.1149+1G>A	ENSP00000414823.2:n.1149+1G>A
ENST00000430669.6:c.1404+1G>A	ENSP00000410287.2:n.1404+1G>A
ENST00000437951.5:c.1404+1G>A	ENSP00000389744.1:n.1404+1G>A
NM_000264.3:c.1602+1G>A , LRG_515t1:c.1602+1G>A	NP_000255.2:n.1602+1G>A
NM_001083602.1:c.1404+1G>A , LRG_515t2:c.1404+1G>A	NP_001077071.1:n.1404+1G>A
NM_001083603.1:c.1599+1G>A	NP_001077072.1:n.1599+1G>A
NM_001083604.1:c.1149+1G>A	NP_001077073.1:n.1149+1G>A
NM_001083605.1:c.1149+1G>A	NP_001077074.1:n.1149+1G>A
NM_001083606.1:c.1149+1G>A	NP_001077075.1:n.1149+1G>A
NM_001083607.1:c.1149+1G>A	NP_001077076.1:n.1149+1G>A
XM_005252102.2:c.1149+1G>A	XP_005252159.1:n.1149+1G>A
XM_011518868.1:c.1446+1G>A	XP_011517170.1:n.1446+1G>A
XM_011518869.1:c.1149+1G>A	XP_011517171.1:n.1149+1G>A
XM_011518870.1:c.1149+1G>A	XP_011517172.1:n.1149+1G>A
XM_011518871.1:c.1149+1G>A	XP_011517173.1:n.1149+1G>A
XM_011518872.1:c.1149+1G>A	XP_011517174.1:n.1149+1G>A
XM_011518873.1:c.762+1G>A	XP_011517175.1:n.762+1G>A
XM_011518874.1:c.1602+1G>A	XP_011517176.1:n.1602+1G>A
NM_000264.4:c.1602+1G>A	NP_000255.2:n.1602+1G>A
NM_001083602.2:c.1404+1G>A	NP_001077071.1:n.1404+1G>A
NM_001083603.2:c.1599+1G>A	NP_001077072.1:n.1599+1G>A
NM_001083604.2:c.1149+1G>A	NP_001077073.1:n.1149+1G>A
NM_001083605.2:c.1149+1G>A	NP_001077074.1:n.1149+1G>A
NM_001083606.2:c.1149+1G>A	NP_001077075.1:n.1149+1G>A
NM_001083607.2:c.1149+1G>A	NP_001077076.1:n.1149+1G>A
NM_001354918.1:c.1446+1G>A	NP_001341847.1:n.1446+1G>A
NR_149061.1:n.1790+1G>A
NM_000264.5:c.1602+1G>A MANE Select	NP_000255.2:n.1602+1G>A
NM_001083606.3:c.1149+1G>A	NP_001077075.1:n.1149+1G>A
NM_001354918.2:c.1446+1G>A	NP_001341847.1:n.1446+1G>A
NR_149061.2:n.2507+1G>A
NM_001083602.3:c.1404+1G>A	NP_001077071.1:n.1404+1G>A
NM_001083603.3:c.1599+1G>A MANE Plus Clinical	NP_001077072.1:n.1599+1G>A
NM_001083604.3:c.1149+1G>A	NP_001077073.1:n.1149+1G>A
NM_001083605.3:c.1149+1G>A	NP_001077074.1:n.1149+1G>A
NM_001083607.3:c.1149+1G>A	NP_001077076.1:n.1149+1G>A