Canonical Allele Identifier: CA5138393

Gene: PTCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95467148A>G , CM000671.2:g.95467148A>G	GRCh38
NC_000009.11:g.98229430A>G , CM000671.1:g.98229430A>G	GRCh37
NC_000009.10:g.97269251A>G	NCBI36
NG_007664.1:g.54818T>C , LRG_515:g.54818T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000264.5:c.2528T>C MANE Select	NP_000255.2:p.Met843Thr
ENST00000331920.11:c.2528T>C MANE Select	ENSP00000332353.6:p.Met843Thr
NM_001083603.3:c.2525T>C MANE Plus Clinical	NP_001077072.1:p.Met842Thr
ENST00000437951.6:c.2525T>C MANE Plus Clinical	ENSP00000389744.2:p.Met842Thr
NM_000264.3:c.2528T>C , LRG_515t1:c.2528T>C	NP_000255.2:p.Met843Thr
NM_000264.4:c.2528T>C	NP_000255.2:p.Met843Thr
NM_001083602.1:c.2330T>C , LRG_515t2:c.2330T>C	NP_001077071.1:p.Met777Thr
NM_001083602.2:c.2330T>C	NP_001077071.1:p.Met777Thr
NM_001083602.3:c.2330T>C	NP_001077071.1:p.Met777Thr
NM_001083603.1:c.2525T>C	NP_001077072.1:p.Met842Thr
NM_001083603.2:c.2525T>C	NP_001077072.1:p.Met842Thr
NM_001083604.1:c.2075T>C	NP_001077073.1:p.Met692Thr
NM_001083604.2:c.2075T>C	NP_001077073.1:p.Met692Thr
NM_001083604.3:c.2075T>C	NP_001077073.1:p.Met692Thr
NM_001083605.1:c.2075T>C	NP_001077074.1:p.Met692Thr
NM_001083605.2:c.2075T>C	NP_001077074.1:p.Met692Thr
NM_001083605.3:c.2075T>C	NP_001077074.1:p.Met692Thr
NM_001083606.1:c.2075T>C	NP_001077075.1:p.Met692Thr
NM_001083606.2:c.2075T>C	NP_001077075.1:p.Met692Thr
NM_001083606.3:c.2075T>C	NP_001077075.1:p.Met692Thr
NM_001083607.1:c.2075T>C	NP_001077076.1:p.Met692Thr
NM_001083607.2:c.2075T>C	NP_001077076.1:p.Met692Thr
NM_001083607.3:c.2075T>C	NP_001077076.1:p.Met692Thr
NM_001354918.1:c.2372T>C	NP_001341847.1:p.Met791Thr
NM_001354918.2:c.2372T>C	NP_001341847.1:p.Met791Thr
NR_038982.1:n.409A>G
NR_149061.1:n.2550T>C
NR_149061.2:n.3267T>C
ENST00000331920.10:c.2528T>C	ENSP00000332353.6:p.Met843Thr
ENST00000375274.6:c.2525T>C	ENSP00000364423.2:p.Met842Thr
ENST00000375290.6:c.2297T>C	ENSP00000364439.2:n.2297T>C
ENST00000418258.5:c.2075T>C	ENSP00000396135.1:p.Met692Thr
ENST00000421141.5:c.2075T>C	ENSP00000399981.1:p.Met692Thr
ENST00000429896.6:c.2075T>C	ENSP00000414823.2:p.Met692Thr
ENST00000430669.6:c.2330T>C	ENSP00000410287.2:p.Met777Thr
ENST00000437951.5:c.2330T>C	ENSP00000389744.1:p.Met777Thr
ENST00000690194.1:c.*836T>C	ENSP00000509379.1:n.*836T>C
ENST00000692981.1:c.2075T>C	ENSP00000510238.1:p.Met692Thr
ENST00000711046.1:c.2330T>C	ENSP00000518556.1:p.Met777Thr
XM_005252102.2:c.2075T>C	XP_005252159.1:p.Met692Thr
XM_011518868.1:c.2372T>C	XP_011517170.1:p.Met791Thr
XM_011518869.1:c.2075T>C	XP_011517171.1:p.Met692Thr
XM_011518870.1:c.2075T>C	XP_011517172.1:p.Met692Thr
XM_011518871.1:c.2075T>C	XP_011517173.1:p.Met692Thr
XM_011518872.1:c.2075T>C	XP_011517174.1:p.Met692Thr
XM_011518873.1:c.1688T>C	XP_011517175.1:p.Met563Thr
XM_011518874.1:c.2528T>C	XP_011517176.1:p.Met843Thr