Canonical Allele Identifier: CA1865591107
Gene: PTCH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95457929A= , CM000671.2:g.95457929A= GRCh38
NC_000009.11:g.98220211A= , CM000671.1:g.98220211A= GRCh37
NC_000009.10:g.97260032A= NCBI36
NG_007664.1:g.64037T= , LRG_515:g.64037T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000711046.1:c.2970+84T= ENSP00000518556.1:n.2970+84T=
ENST00000437951.6:c.3165+84T= MANE Plus Clinical ENSP00000389744.2:n.3165+84T=
ENST00000690194.1:c.*1476+84T= ENSP00000509379.1:n.*1476+84T=
ENST00000692981.1:c.2715+84T= ENSP00000510238.1:n.2715+84T=
ENST00000693534.1:n.499+84T=
ENST00000331920.11:c.3168+84T= MANE Select ENSP00000332353.6:n.3168+84T=
ENST00000331920.10:c.3168+84T= ENSP00000332353.6:n.3168+84T=
ENST00000375274.6:c.3165+84T= ENSP00000364423.2:n.3165+84T=
ENST00000375290.6:c.2937+84T= ENSP00000364439.2:n.2937+84T=
ENST00000418258.5:c.2715+84T= ENSP00000396135.1:n.2715+84T=
ENST00000421141.5:c.2715+84T= ENSP00000399981.1:n.2715+84T=
ENST00000429896.6:c.2715+84T= ENSP00000414823.2:n.2715+84T=
ENST00000430669.6:c.2970+84T= ENSP00000410287.2:n.2970+84T=
ENST00000437951.5:c.2970+84T= ENSP00000389744.1:n.2970+84T=
ENST00000547615.1:n.518+84T=
NM_000264.3:c.3168+84T= , LRG_515t1:c.3168+84T= NP_000255.2:n.3168+84T=
NM_001083602.1:c.2970+84T= , LRG_515t2:c.2970+84T= NP_001077071.1:n.2970+84T=
NM_001083603.1:c.3165+84T= NP_001077072.1:n.3165+84T=
NM_001083604.1:c.2715+84T= NP_001077073.1:n.2715+84T=
NM_001083605.1:c.2715+84T= NP_001077074.1:n.2715+84T=
NM_001083606.1:c.2715+84T= NP_001077075.1:n.2715+84T=
NM_001083607.1:c.2715+84T= NP_001077076.1:n.2715+84T=
XM_005252102.2:c.2715+84T= XP_005252159.1:n.2715+84T=
XM_011518868.1:c.3012+84T= XP_011517170.1:n.3012+84T=
XM_011518869.1:c.2715+84T= XP_011517171.1:n.2715+84T=
XM_011518870.1:c.2715+84T= XP_011517172.1:n.2715+84T=
XM_011518871.1:c.2715+84T= XP_011517173.1:n.2715+84T=
XM_011518872.1:c.2715+84T= XP_011517174.1:n.2715+84T=
XM_011518873.1:c.2328+84T= XP_011517175.1:n.2328+84T=
XM_011518874.1:c.3168+84T= XP_011517176.1:n.3168+84T=
NM_000264.4:c.3168+84T= NP_000255.2:n.3168+84T=
NM_001083602.2:c.2970+84T= NP_001077071.1:n.2970+84T=
NM_001083603.2:c.3165+84T= NP_001077072.1:n.3165+84T=
NM_001083604.2:c.2715+84T= NP_001077073.1:n.2715+84T=
NM_001083605.2:c.2715+84T= NP_001077074.1:n.2715+84T=
NM_001083606.2:c.2715+84T= NP_001077075.1:n.2715+84T=
NM_001083607.2:c.2715+84T= NP_001077076.1:n.2715+84T=
NM_001354918.1:c.3012+84T= NP_001341847.1:n.3012+84T=
NR_149061.1:n.3190+84T=
NM_000264.5:c.3168+84T= MANE Select NP_000255.2:n.3168+84T=
NM_001083606.3:c.2715+84T= NP_001077075.1:n.2715+84T=
NM_001354918.2:c.3012+84T= NP_001341847.1:n.3012+84T=
NR_149061.2:n.3907+84T=
NM_001083602.3:c.2970+84T= NP_001077071.1:n.2970+84T=
NM_001083603.3:c.3165+84T= MANE Plus Clinical NP_001077072.1:n.3165+84T=
NM_001083604.3:c.2715+84T= NP_001077073.1:n.2715+84T=
NM_001083605.3:c.2715+84T= NP_001077074.1:n.2715+84T=
NM_001083607.3:c.2715+84T= NP_001077076.1:n.2715+84T=