Canonical Allele Identifier: CA16618909
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 419592
dbSNP Id: rs1064793978

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95477704T>C , CM000671.2:g.95477704T>C GRCh38
NC_000009.11:g.98239986T>C , CM000671.1:g.98239986T>C GRCh37
NC_000009.10:g.97279807T>C NCBI36
NG_007664.1:g.44262A>G , LRG_515:g.44262A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000711046.1:c.1150-2A>G ENSP00000518556.1:n.1150-2A>G
ENST00000437951.6:c.1345-2A>G MANE Plus Clinical ENSP00000389744.2:n.1345-2A>G
ENST00000690194.1:c.895-2A>G ENSP00000509379.1:n.895-2A>G
ENST00000692981.1:c.895-2A>G ENSP00000510238.1:n.895-2A>G
ENST00000331920.11:c.1348-2A>G MANE Select ENSP00000332353.6:n.1348-2A>G
ENST00000331920.10:c.1348-2A>G ENSP00000332353.6:n.1348-2A>G
ENST00000375271.4:c.498+351A>G ENSP00000364420.4:n.498+351A>G
ENST00000375274.6:c.1345-2A>G ENSP00000364423.2:n.1345-2A>G
ENST00000375290.6:c.985-2A>G ENSP00000364439.2:n.985-2A>G
ENST00000418258.5:c.895-2A>G ENSP00000396135.1:n.895-2A>G
ENST00000421141.5:c.895-2A>G ENSP00000399981.1:n.895-2A>G
ENST00000429896.6:c.895-2A>G ENSP00000414823.2:n.895-2A>G
ENST00000430669.6:c.1150-2A>G ENSP00000410287.2:n.1150-2A>G
ENST00000437951.5:c.1150-2A>G ENSP00000389744.1:n.1150-2A>G
NM_000264.3:c.1348-2A>G , LRG_515t1:c.1348-2A>G NP_000255.2:n.1348-2A>G
NM_001083602.1:c.1150-2A>G , LRG_515t2:c.1150-2A>G NP_001077071.1:n.1150-2A>G
NM_001083603.1:c.1345-2A>G NP_001077072.1:n.1345-2A>G
NM_001083604.1:c.895-2A>G NP_001077073.1:n.895-2A>G
NM_001083605.1:c.895-2A>G NP_001077074.1:n.895-2A>G
NM_001083606.1:c.895-2A>G NP_001077075.1:n.895-2A>G
NM_001083607.1:c.895-2A>G NP_001077076.1:n.895-2A>G
XM_005252102.2:c.895-2A>G XP_005252159.1:n.895-2A>G
XM_011518868.1:c.1347+351A>G XP_011517170.1:n.1347+351A>G
XM_011518869.1:c.895-2A>G XP_011517171.1:n.895-2A>G
XM_011518870.1:c.895-2A>G XP_011517172.1:n.895-2A>G
XM_011518871.1:c.895-2A>G XP_011517173.1:n.895-2A>G
XM_011518872.1:c.895-2A>G XP_011517174.1:n.895-2A>G
XM_011518873.1:c.508-2A>G XP_011517175.1:n.508-2A>G
XM_011518874.1:c.1348-2A>G XP_011517176.1:n.1348-2A>G
NM_000264.4:c.1348-2A>G NP_000255.2:n.1348-2A>G
NM_001083602.2:c.1150-2A>G NP_001077071.1:n.1150-2A>G
NM_001083603.2:c.1345-2A>G NP_001077072.1:n.1345-2A>G
NM_001083604.2:c.895-2A>G NP_001077073.1:n.895-2A>G
NM_001083605.2:c.895-2A>G NP_001077074.1:n.895-2A>G
NM_001083606.2:c.895-2A>G NP_001077075.1:n.895-2A>G
NM_001083607.2:c.895-2A>G NP_001077076.1:n.895-2A>G
NM_001354918.1:c.1347+351A>G NP_001341847.1:n.1347+351A>G
NR_149061.1:n.1536-2A>G
NM_000264.5:c.1348-2A>G MANE Select NP_000255.2:n.1348-2A>G
NM_001083606.3:c.895-2A>G NP_001077075.1:n.895-2A>G
NM_001354918.2:c.1347+351A>G NP_001341847.1:n.1347+351A>G
NR_149061.2:n.2253-2A>G
NM_001083602.3:c.1150-2A>G NP_001077071.1:n.1150-2A>G
NM_001083603.3:c.1345-2A>G MANE Plus Clinical NP_001077072.1:n.1345-2A>G
NM_001083604.3:c.895-2A>G NP_001077073.1:n.895-2A>G
NM_001083605.3:c.895-2A>G NP_001077074.1:n.895-2A>G
NM_001083607.3:c.895-2A>G NP_001077076.1:n.895-2A>G