Canonical Allele Identifier: CA915947072

Gene: PTCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95449180_95449181delinsTG , CM000671.2:g.95449180_95449181delinsTG	GRCh38
NC_000009.11:g.98211462_98211463delinsTG , CM000671.1:g.98211462_98211463delinsTG	GRCh37
NC_000009.10:g.97251283_97251284delinsTG	NCBI36
NG_007664.1:g.72785_72786delinsCA , LRG_515:g.72785_72786delinsCA

Transcript Alleles

HGVS	Amino-acid Change
NM_000264.5:c.3692_3693delinsCA MANE Select	NP_000255.2:p.Val1231Ala
ENST00000331920.11:c.3692_3693delinsCA MANE Select	ENSP00000332353.6:p.Val1231Ala
NM_001083603.3:c.3689_3690delinsCA MANE Plus Clinical	NP_001077072.1:p.Val1230Ala
ENST00000437951.6:c.3689_3690delinsCA MANE Plus Clinical	ENSP00000389744.2:p.Val1230Ala
NM_000264.3:c.3692_3693delinsCA , LRG_515t1:c.3692_3693delinsCA	NP_000255.2:p.Val1231Ala
NM_000264.4:c.3692_3693delinsCA	NP_000255.2:p.Val1231Ala
NM_001083602.1:c.3494_3495delinsCA , LRG_515t2:c.3494_3495delinsCA	NP_001077071.1:p.Val1165Ala
NM_001083602.2:c.3494_3495delinsCA	NP_001077071.1:p.Val1165Ala
NM_001083602.3:c.3494_3495delinsCA	NP_001077071.1:p.Val1165Ala
NM_001083603.1:c.3689_3690delinsCA	NP_001077072.1:p.Val1230Ala
NM_001083603.2:c.3689_3690delinsCA	NP_001077072.1:p.Val1230Ala
NM_001083604.1:c.3239_3240delinsCA	NP_001077073.1:p.Val1080Ala
NM_001083604.2:c.3239_3240delinsCA	NP_001077073.1:p.Val1080Ala
NM_001083604.3:c.3239_3240delinsCA	NP_001077073.1:p.Val1080Ala
NM_001083605.1:c.3239_3240delinsCA	NP_001077074.1:p.Val1080Ala
NM_001083605.2:c.3239_3240delinsCA	NP_001077074.1:p.Val1080Ala
NM_001083605.3:c.3239_3240delinsCA	NP_001077074.1:p.Val1080Ala
NM_001083606.1:c.3239_3240delinsCA	NP_001077075.1:p.Val1080Ala
NM_001083606.2:c.3239_3240delinsCA	NP_001077075.1:p.Val1080Ala
NM_001083606.3:c.3239_3240delinsCA	NP_001077075.1:p.Val1080Ala
NM_001083607.1:c.3239_3240delinsCA	NP_001077076.1:p.Val1080Ala
NM_001083607.2:c.3239_3240delinsCA	NP_001077076.1:p.Val1080Ala
NM_001083607.3:c.3239_3240delinsCA	NP_001077076.1:p.Val1080Ala
NM_001354918.1:c.3536_3537delinsCA	NP_001341847.1:p.Val1179Ala
NM_001354918.2:c.3536_3537delinsCA	NP_001341847.1:p.Val1179Ala
NR_149061.1:n.3714_3715delinsCA
NR_149061.2:n.4431_4432delinsCA
ENST00000331920.10:c.3692_3693delinsCA	ENSP00000332353.6:p.Val1231Ala
ENST00000375274.6:c.3689_3690delinsCA	ENSP00000364423.2:p.Val1230Ala
ENST00000375290.6:c.6998_6999delinsCA	ENSP00000364439.2:n.6998_6999delinsCA
ENST00000418258.5:c.3239_3240delinsCA	ENSP00000396135.1:p.Val1080Ala
ENST00000421141.5:c.3239_3240delinsCA	ENSP00000399981.1:p.Val1080Ala
ENST00000429896.6:c.3239_3240delinsCA	ENSP00000414823.2:p.Val1080Ala
ENST00000430669.6:c.3494_3495delinsCA	ENSP00000410287.2:p.Val1165Ala
ENST00000437951.5:c.3494_3495delinsCA	ENSP00000389744.1:p.Val1165Ala
ENST00000546744.5:n.756_757delinsCA
ENST00000687744.1:n.1889_1890delinsCA
ENST00000690194.1:c.*2000_*2001delinsCA	ENSP00000509379.1:n.*2000_*2001delinsCA
ENST00000692981.1:c.3239_3240delinsCA	ENSP00000510238.1:p.Val1080Ala
ENST00000693534.1:n.1039_1040delinsCA
ENST00000711046.1:c.3494_3495delinsCA	ENSP00000518556.1:p.Val1165Ala
XM_005252102.2:c.3239_3240delinsCA	XP_005252159.1:p.Val1080Ala
XM_011518868.1:c.3536_3537delinsCA	XP_011517170.1:p.Val1179Ala
XM_011518869.1:c.3239_3240delinsCA	XP_011517171.1:p.Val1080Ala
XM_011518870.1:c.3239_3240delinsCA	XP_011517172.1:p.Val1080Ala
XM_011518871.1:c.3239_3240delinsCA	XP_011517173.1:p.Val1080Ala
XM_011518872.1:c.3239_3240delinsCA	XP_011517174.1:p.Val1080Ala
XM_011518873.1:c.2852_2853delinsCA	XP_011517175.1:p.Val951Ala