Canonical Allele Identifier: CA1865583658

Gene: PTCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95453497_95453499delinsCAG , CM000671.2:g.95453497_95453499delinsCAG	GRCh38
NC_000009.11:g.98215779_98215781delinsCAG , CM000671.1:g.98215779_98215781delinsCAG	GRCh37
NC_000009.10:g.97255600_97255602delinsCAG	NCBI36
NG_007664.1:g.68467_68469delinsCTG , LRG_515:g.68467_68469delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711046.1:c.3230_3232delinsCTG	ENSP00000518556.1:p.Ser1077=
ENST00000437951.6:c.3425_3427delinsCTG MANE Plus Clinical	ENSP00000389744.2:p.Ser1142=
ENST00000690194.1:c.*1736_*1738delinsCTG	ENSP00000509379.1:n.*1736_*1738delinsCTG
ENST00000692981.1:c.2975_2977delinsCTG	ENSP00000510238.1:p.Ser992=
ENST00000693534.1:n.759_761delinsCTG
ENST00000331920.11:c.3428_3430delinsCTG MANE Select	ENSP00000332353.6:p.Ser1143=
ENST00000331920.10:c.3428_3430delinsCTG	ENSP00000332353.6:p.Ser1143=
ENST00000375274.6:c.3425_3427delinsCTG	ENSP00000364423.2:p.Ser1142=
ENST00000375290.6:c.3197_3199delinsCTG	ENSP00000364439.2:n.3197_3199delinsCTG
ENST00000418258.5:c.2975_2977delinsCTG	ENSP00000396135.1:p.Ser992=
ENST00000421141.5:c.2975_2977delinsCTG	ENSP00000399981.1:p.Ser992=
ENST00000429896.6:c.2975_2977delinsCTG	ENSP00000414823.2:p.Ser992=
ENST00000430669.6:c.3230_3232delinsCTG	ENSP00000410287.2:p.Ser1077=
ENST00000437951.5:c.3230_3232delinsCTG	ENSP00000389744.1:p.Ser1077=
NM_000264.3:c.3428_3430delinsCTG , LRG_515t1:c.3428_3430delinsCTG	NP_000255.2:p.Ser1143=
NM_001083602.1:c.3230_3232delinsCTG , LRG_515t2:c.3230_3232delinsCTG	NP_001077071.1:p.Ser1077=
NM_001083603.1:c.3425_3427delinsCTG	NP_001077072.1:p.Ser1142=
NM_001083604.1:c.2975_2977delinsCTG	NP_001077073.1:p.Ser992=
NM_001083605.1:c.2975_2977delinsCTG	NP_001077074.1:p.Ser992=
NM_001083606.1:c.2975_2977delinsCTG	NP_001077075.1:p.Ser992=
NM_001083607.1:c.2975_2977delinsCTG	NP_001077076.1:p.Ser992=
XM_005252102.2:c.2975_2977delinsCTG	XP_005252159.1:p.Ser992=
XM_011518868.1:c.3272_3274delinsCTG	XP_011517170.1:p.Ser1091=
XM_011518869.1:c.2975_2977delinsCTG	XP_011517171.1:p.Ser992=
XM_011518870.1:c.2975_2977delinsCTG	XP_011517172.1:p.Ser992=
XM_011518871.1:c.2975_2977delinsCTG	XP_011517173.1:p.Ser992=
XM_011518872.1:c.2975_2977delinsCTG	XP_011517174.1:p.Ser992=
XM_011518873.1:c.2588_2590delinsCTG	XP_011517175.1:p.Ser863=
XM_011518874.1:c.3428_3430delinsCTG	XP_011517176.1:p.Ser1143=
NM_000264.4:c.3428_3430delinsCTG	NP_000255.2:p.Ser1143=
NM_001083602.2:c.3230_3232delinsCTG	NP_001077071.1:p.Ser1077=
NM_001083603.2:c.3425_3427delinsCTG	NP_001077072.1:p.Ser1142=
NM_001083604.2:c.2975_2977delinsCTG	NP_001077073.1:p.Ser992=
NM_001083605.2:c.2975_2977delinsCTG	NP_001077074.1:p.Ser992=
NM_001083606.2:c.2975_2977delinsCTG	NP_001077075.1:p.Ser992=
NM_001083607.2:c.2975_2977delinsCTG	NP_001077076.1:p.Ser992=
NM_001354918.1:c.3272_3274delinsCTG	NP_001341847.1:p.Ser1091=
NR_149061.1:n.3450_3452delinsCTG
NM_000264.5:c.3428_3430delinsCTG MANE Select	NP_000255.2:p.Ser1143=
NM_001083606.3:c.2975_2977delinsCTG	NP_001077075.1:p.Ser992=
NM_001354918.2:c.3272_3274delinsCTG	NP_001341847.1:p.Ser1091=
NR_149061.2:n.4167_4169delinsCTG
NM_001083602.3:c.3230_3232delinsCTG	NP_001077071.1:p.Ser1077=
NM_001083603.3:c.3425_3427delinsCTG MANE Plus Clinical	NP_001077072.1:p.Ser1142=
NM_001083604.3:c.2975_2977delinsCTG	NP_001077073.1:p.Ser992=
NM_001083605.3:c.2975_2977delinsCTG	NP_001077074.1:p.Ser992=
NM_001083607.3:c.2975_2977delinsCTG	NP_001077076.1:p.Ser992=