Canonical Allele Identifier: CA16612928

Gene: PTCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95468827G>C , CM000671.2:g.95468827G>C	GRCh38
NC_000009.11:g.98231109G>C , CM000671.1:g.98231109G>C	GRCh37
NC_000009.10:g.97270930G>C	NCBI36
NG_007664.1:g.53139C>G , LRG_515:g.53139C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000264.5:c.2174C>G MANE Select	NP_000255.2:p.Pro725Arg
ENST00000331920.11:c.2174C>G MANE Select	ENSP00000332353.6:p.Pro725Arg
NM_001083603.3:c.2171C>G MANE Plus Clinical	NP_001077072.1:p.Pro724Arg
ENST00000437951.6:c.2171C>G MANE Plus Clinical	ENSP00000389744.2:p.Pro724Arg
NM_000264.3:c.2174C>G , LRG_515t1:c.2174C>G	NP_000255.2:p.Pro725Arg
NM_000264.4:c.2174C>G	NP_000255.2:p.Pro725Arg
NM_001083602.1:c.1976C>G , LRG_515t2:c.1976C>G	NP_001077071.1:p.Pro659Arg
NM_001083602.2:c.1976C>G	NP_001077071.1:p.Pro659Arg
NM_001083602.3:c.1976C>G	NP_001077071.1:p.Pro659Arg
NM_001083603.1:c.2171C>G	NP_001077072.1:p.Pro724Arg
NM_001083603.2:c.2171C>G	NP_001077072.1:p.Pro724Arg
NM_001083604.1:c.1721C>G	NP_001077073.1:p.Pro574Arg
NM_001083604.2:c.1721C>G	NP_001077073.1:p.Pro574Arg
NM_001083604.3:c.1721C>G	NP_001077073.1:p.Pro574Arg
NM_001083605.1:c.1721C>G	NP_001077074.1:p.Pro574Arg
NM_001083605.2:c.1721C>G	NP_001077074.1:p.Pro574Arg
NM_001083605.3:c.1721C>G	NP_001077074.1:p.Pro574Arg
NM_001083606.1:c.1721C>G	NP_001077075.1:p.Pro574Arg
NM_001083606.2:c.1721C>G	NP_001077075.1:p.Pro574Arg
NM_001083606.3:c.1721C>G	NP_001077075.1:p.Pro574Arg
NM_001083607.1:c.1721C>G	NP_001077076.1:p.Pro574Arg
NM_001083607.2:c.1721C>G	NP_001077076.1:p.Pro574Arg
NM_001083607.3:c.1721C>G	NP_001077076.1:p.Pro574Arg
NM_001354918.1:c.2018C>G	NP_001341847.1:p.Pro673Arg
NM_001354918.2:c.2018C>G	NP_001341847.1:p.Pro673Arg
NR_038982.1:n.765G>C
NR_149061.1:n.2362C>G
NR_149061.2:n.3079C>G
ENST00000331920.10:c.2174C>G	ENSP00000332353.6:p.Pro725Arg
ENST00000375274.6:c.2171C>G	ENSP00000364423.2:p.Pro724Arg
ENST00000375290.6:c.1943C>G	ENSP00000364439.2:n.1943C>G
ENST00000418258.5:c.1721C>G	ENSP00000396135.1:p.Pro574Arg
ENST00000421141.5:c.1721C>G	ENSP00000399981.1:p.Pro574Arg
ENST00000429896.6:c.1721C>G	ENSP00000414823.2:p.Pro574Arg
ENST00000430669.6:c.1976C>G	ENSP00000410287.2:p.Pro659Arg
ENST00000437951.5:c.1976C>G	ENSP00000389744.1:p.Pro659Arg
ENST00000549678.1:n.363C>G
ENST00000690194.1:c.*482C>G	ENSP00000509379.1:n.*482C>G
ENST00000692981.1:c.1721C>G	ENSP00000510238.1:p.Pro574Arg
ENST00000711046.1:c.1976C>G	ENSP00000518556.1:p.Pro659Arg
XM_005252102.2:c.1721C>G	XP_005252159.1:p.Pro574Arg
XM_011518868.1:c.2018C>G	XP_011517170.1:p.Pro673Arg
XM_011518869.1:c.1721C>G	XP_011517171.1:p.Pro574Arg
XM_011518870.1:c.1721C>G	XP_011517172.1:p.Pro574Arg
XM_011518871.1:c.1721C>G	XP_011517173.1:p.Pro574Arg
XM_011518872.1:c.1721C>G	XP_011517174.1:p.Pro574Arg
XM_011518873.1:c.1334C>G	XP_011517175.1:p.Pro445Arg
XM_011518874.1:c.2174C>G	XP_011517176.1:p.Pro725Arg