Canonical Allele Identifier: CA2690800836

Gene: PTCH1

Linked Data

• gnomAD v4: 9-95457938-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95457941_95457942del , CM000671.2:g.95457941_95457942del	GRCh38
NC_000009.11:g.98220223_98220224del , CM000671.1:g.98220223_98220224del	GRCh37
NC_000009.10:g.97260044_97260045del	NCBI36
NG_007664.1:g.64026_64027del , LRG_515:g.64026_64027del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711046.1:c.2970+73_2970+74del	ENSP00000518556.1:n.2970+73_2970+74del
ENST00000437951.6:c.3165+73_3165+74del MANE Plus Clinical	ENSP00000389744.2:n.3165+73_3165+74del
ENST00000690194.1:c.*1476+73_*1476+74del	ENSP00000509379.1:n.*1476+73_*1476+74del
ENST00000692981.1:c.2715+73_2715+74del	ENSP00000510238.1:n.2715+73_2715+74del
ENST00000693534.1:n.499+73_499+74del
ENST00000331920.11:c.3168+73_3168+74del MANE Select	ENSP00000332353.6:n.3168+73_3168+74del
ENST00000331920.10:c.3168+73_3168+74del	ENSP00000332353.6:n.3168+73_3168+74del
ENST00000375274.6:c.3165+73_3165+74del	ENSP00000364423.2:n.3165+73_3165+74del
ENST00000375290.6:c.2937+73_2937+74del	ENSP00000364439.2:n.2937+73_2937+74del
ENST00000418258.5:c.2715+73_2715+74del	ENSP00000396135.1:n.2715+73_2715+74del
ENST00000421141.5:c.2715+73_2715+74del	ENSP00000399981.1:n.2715+73_2715+74del
ENST00000429896.6:c.2715+73_2715+74del	ENSP00000414823.2:n.2715+73_2715+74del
ENST00000430669.6:c.2970+73_2970+74del	ENSP00000410287.2:n.2970+73_2970+74del
ENST00000437951.5:c.2970+73_2970+74del	ENSP00000389744.1:n.2970+73_2970+74del
ENST00000547615.1:n.518+73_518+74del
NM_000264.3:c.3168+73_3168+74del , LRG_515t1:c.3168+73_3168+74del	NP_000255.2:n.3168+73_3168+74del
NM_001083602.1:c.2970+73_2970+74del , LRG_515t2:c.2970+73_2970+74del	NP_001077071.1:n.2970+73_2970+74del
NM_001083603.1:c.3165+73_3165+74del	NP_001077072.1:n.3165+73_3165+74del
NM_001083604.1:c.2715+73_2715+74del	NP_001077073.1:n.2715+73_2715+74del
NM_001083605.1:c.2715+73_2715+74del	NP_001077074.1:n.2715+73_2715+74del
NM_001083606.1:c.2715+73_2715+74del	NP_001077075.1:n.2715+73_2715+74del
NM_001083607.1:c.2715+73_2715+74del	NP_001077076.1:n.2715+73_2715+74del
XM_005252102.2:c.2715+73_2715+74del	XP_005252159.1:n.2715+73_2715+74del
XM_011518868.1:c.3012+73_3012+74del	XP_011517170.1:n.3012+73_3012+74del
XM_011518869.1:c.2715+73_2715+74del	XP_011517171.1:n.2715+73_2715+74del
XM_011518870.1:c.2715+73_2715+74del	XP_011517172.1:n.2715+73_2715+74del
XM_011518871.1:c.2715+73_2715+74del	XP_011517173.1:n.2715+73_2715+74del
XM_011518872.1:c.2715+73_2715+74del	XP_011517174.1:n.2715+73_2715+74del
XM_011518873.1:c.2328+73_2328+74del	XP_011517175.1:n.2328+73_2328+74del
XM_011518874.1:c.3168+73_3168+74del	XP_011517176.1:n.3168+73_3168+74del
NM_000264.4:c.3168+73_3168+74del	NP_000255.2:n.3168+73_3168+74del
NM_001083602.2:c.2970+73_2970+74del	NP_001077071.1:n.2970+73_2970+74del
NM_001083603.2:c.3165+73_3165+74del	NP_001077072.1:n.3165+73_3165+74del
NM_001083604.2:c.2715+73_2715+74del	NP_001077073.1:n.2715+73_2715+74del
NM_001083605.2:c.2715+73_2715+74del	NP_001077074.1:n.2715+73_2715+74del
NM_001083606.2:c.2715+73_2715+74del	NP_001077075.1:n.2715+73_2715+74del
NM_001083607.2:c.2715+73_2715+74del	NP_001077076.1:n.2715+73_2715+74del
NM_001354918.1:c.3012+73_3012+74del	NP_001341847.1:n.3012+73_3012+74del
NR_149061.1:n.3190+73_3190+74del
NM_000264.5:c.3168+73_3168+74del MANE Select	NP_000255.2:n.3168+73_3168+74del
NM_001083606.3:c.2715+73_2715+74del	NP_001077075.1:n.2715+73_2715+74del
NM_001354918.2:c.3012+73_3012+74del	NP_001341847.1:n.3012+73_3012+74del
NR_149061.2:n.3907+73_3907+74del
NM_001083602.3:c.2970+73_2970+74del	NP_001077071.1:n.2970+73_2970+74del
NM_001083603.3:c.3165+73_3165+74del MANE Plus Clinical	NP_001077072.1:n.3165+73_3165+74del
NM_001083604.3:c.2715+73_2715+74del	NP_001077073.1:n.2715+73_2715+74del
NM_001083605.3:c.2715+73_2715+74del	NP_001077074.1:n.2715+73_2715+74del
NM_001083607.3:c.2715+73_2715+74del	NP_001077076.1:n.2715+73_2715+74del