Canonical Allele Identifier: CA374115012

Gene: PTCH1

Linked Data

• dbSNP Id: rs1841591077
• COSMIC: COSM5923851 ; COSM5923852 ; COSM5923853 ; COSM5923854
• MyVariant Identifiers: chr9:g.98244418G>A (hg19) ; chr9:g.95482136G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95482136G>A , CM000671.2:g.95482136G>A	GRCh38
NC_000009.11:g.98244418G>A , CM000671.1:g.98244418G>A	GRCh37
NC_000009.10:g.97284239G>A	NCBI36
NG_007664.1:g.39830C>T , LRG_515:g.39830C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711046.1:c.454C>T	ENSP00000518556.1:p.Gln152Ter
ENST00000437951.6:c.649C>T MANE Plus Clinical	ENSP00000389744.2:p.Gln217Ter
ENST00000690194.1:c.199C>T	ENSP00000509379.1:p.Gln67Ter
ENST00000692981.1:c.199C>T	ENSP00000510238.1:p.Gln67Ter
ENST00000331920.11:c.652C>T MANE Select	ENSP00000332353.6:p.Gln218Ter
ENST00000331920.10:c.652C>T	ENSP00000332353.6:p.Gln218Ter
ENST00000375274.6:c.649C>T	ENSP00000364423.2:p.Gln217Ter
ENST00000375290.6:c.384-1548C>T	ENSP00000364439.2:n.384-1548C>T
ENST00000418258.5:c.199C>T	ENSP00000396135.1:p.Gln67Ter
ENST00000421141.5:c.199C>T	ENSP00000399981.1:p.Gln67Ter
ENST00000429896.6:c.199C>T	ENSP00000414823.2:p.Gln67Ter
ENST00000430669.6:c.454C>T	ENSP00000410287.2:p.Gln152Ter
ENST00000437951.5:c.454C>T	ENSP00000389744.1:p.Gln152Ter
ENST00000468211.6:c.454C>T	ENSP00000449745.1:p.Gln152Ter
ENST00000546820.5:c.199C>T	ENSP00000448843.1:p.Gln67Ter
ENST00000547672.5:c.199C>T	ENSP00000447878.1:p.Gln67Ter
ENST00000548379.5:n.305C>T
ENST00000548420.1:c.-94-1548C>T	ENSP00000449078.1:n.-94-1548C>T
ENST00000548945.6:n.194-1548C>T
ENST00000550136.1:n.2174C>T
ENST00000550914.6:c.234C>T	ENSP00000450047.1:p.Ile78=
ENST00000551623.1:c.294C>T	ENSP00000447242.1:n.294C>T
ENST00000551630.1:c.199C>T	ENSP00000450131.1:p.Gln67Ter
ENST00000551845.5:c.199C>T	ENSP00000447008.1:p.Gln67Ter
ENST00000553011.5:c.199C>T	ENSP00000447797.1:p.Gln67Ter
ENST00000553256.5:n.398C>T
NM_000264.3:c.652C>T , LRG_515t1:c.652C>T	NP_000255.2:p.Gln218Ter
NM_001083602.1:c.454C>T , LRG_515t2:c.454C>T	NP_001077071.1:p.Gln152Ter
NM_001083603.1:c.649C>T	NP_001077072.1:p.Gln217Ter
NM_001083604.1:c.199C>T	NP_001077073.1:p.Gln67Ter
NM_001083605.1:c.199C>T	NP_001077074.1:p.Gln67Ter
NM_001083606.1:c.199C>T	NP_001077075.1:p.Gln67Ter
NM_001083607.1:c.199C>T	NP_001077076.1:p.Gln67Ter
XM_005252102.2:c.199C>T	XP_005252159.1:p.Gln67Ter
XM_011518868.1:c.652C>T	XP_011517170.1:p.Gln218Ter
XM_011518869.1:c.199C>T	XP_011517171.1:p.Gln67Ter
XM_011518870.1:c.199C>T	XP_011517172.1:p.Gln67Ter
XM_011518871.1:c.199C>T	XP_011517173.1:p.Gln67Ter
XM_011518872.1:c.199C>T	XP_011517174.1:p.Gln67Ter
XM_011518873.1:c.-94-1548C>T	XP_011517175.1:n.-94-1548C>T
XM_011518874.1:c.652C>T	XP_011517176.1:p.Gln218Ter
NM_000264.4:c.652C>T	NP_000255.2:p.Gln218Ter
NM_001083602.2:c.454C>T	NP_001077071.1:p.Gln152Ter
NM_001083603.2:c.649C>T	NP_001077072.1:p.Gln217Ter
NM_001083604.2:c.199C>T	NP_001077073.1:p.Gln67Ter
NM_001083605.2:c.199C>T	NP_001077074.1:p.Gln67Ter
NM_001083606.2:c.199C>T	NP_001077075.1:p.Gln67Ter
NM_001083607.2:c.199C>T	NP_001077076.1:p.Gln67Ter
NM_001354918.1:c.652C>T	NP_001341847.1:p.Gln218Ter
NM_001354919.1:c.454C>T	NP_001341848.1:p.Gln152Ter
NR_149061.1:n.840C>T
NM_000264.5:c.652C>T MANE Select	NP_000255.2:p.Gln218Ter
NM_001083606.3:c.199C>T	NP_001077075.1:p.Gln67Ter
NM_001354918.2:c.652C>T	NP_001341847.1:p.Gln218Ter
NR_149061.2:n.1557C>T
NM_001083602.3:c.454C>T	NP_001077071.1:p.Gln152Ter
NM_001083603.3:c.649C>T MANE Plus Clinical	NP_001077072.1:p.Gln217Ter
NM_001083604.3:c.199C>T	NP_001077073.1:p.Gln67Ter
NM_001083605.3:c.199C>T	NP_001077074.1:p.Gln67Ter
NM_001083607.3:c.199C>T	NP_001077076.1:p.Gln67Ter
NM_001354919.2:c.454C>T	NP_001341848.1:p.Gln152Ter