Canonical Allele Identifier: CA374120145
Community Standard Title: NM_000264.5(PTCH1):c.387G>A (p.Trp129Ter)
Gene: PTCH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95506414C>T , CM000671.2:g.95506414C>T GRCh38
NC_000009.11:g.98268696C>T , CM000671.1:g.98268696C>T GRCh37
NC_000009.10:g.97308517C>T NCBI36
NG_007664.1:g.15552G>A , LRG_515:g.15552G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000264.5:c.387G>A MANE Select NP_000255.2:p.Trp129Ter
ENST00000331920.11:c.387G>A MANE Select ENSP00000332353.6:p.Trp129Ter
NM_001083603.3:c.384G>A MANE Plus Clinical NP_001077072.1:p.Trp128Ter
ENST00000437951.6:c.384G>A MANE Plus Clinical ENSP00000389744.2:p.Trp128Ter
NM_000264.3:c.387G>A , LRG_515t1:c.387G>A NP_000255.2:p.Trp129Ter
NM_000264.4:c.387G>A NP_000255.2:p.Trp129Ter
NM_001083602.1:c.189G>A , LRG_515t2:c.189G>A NP_001077071.1:p.Trp63Ter
NM_001083602.2:c.189G>A NP_001077071.1:p.Trp63Ter
NM_001083602.3:c.189G>A NP_001077071.1:p.Trp63Ter
NM_001083603.1:c.384G>A NP_001077072.1:p.Trp128Ter
NM_001083603.2:c.384G>A NP_001077072.1:p.Trp128Ter
NM_001083604.1:c.-67G>A NP_001077073.1:n.-67G>A
NM_001083604.2:c.-67G>A NP_001077073.1:n.-67G>A
NM_001083604.3:c.-67G>A NP_001077073.1:n.-67G>A
NM_001083605.1:c.-67G>A NP_001077074.1:n.-67G>A
NM_001083605.2:c.-67G>A NP_001077074.1:n.-67G>A
NM_001083605.3:c.-67G>A NP_001077074.1:n.-67G>A
NM_001083606.1:c.-67G>A NP_001077075.1:n.-67G>A
NM_001083606.2:c.-67G>A NP_001077075.1:n.-67G>A
NM_001083606.3:c.-67G>A NP_001077075.1:n.-67G>A
NM_001083607.1:c.-67G>A NP_001077076.1:n.-67G>A
NM_001083607.2:c.-67G>A NP_001077076.1:n.-67G>A
NM_001083607.3:c.-67G>A NP_001077076.1:n.-67G>A
NM_001354918.1:c.387G>A NP_001341847.1:p.Trp129Ter
NM_001354918.2:c.387G>A NP_001341847.1:p.Trp129Ter
NM_001354919.1:c.189G>A NP_001341848.1:p.Trp63Ter
NM_001354919.2:c.189G>A NP_001341848.1:p.Trp63Ter
NR_149061.1:n.575G>A
NR_149061.2:n.1292G>A
ENST00000331920.10:c.387G>A ENSP00000332353.6:p.Trp129Ter
ENST00000375274.6:c.384G>A ENSP00000364423.2:p.Trp128Ter
ENST00000375290.6:c.186G>A ENSP00000364439.2:p.Trp62Ter
ENST00000418258.5:c.-67G>A ENSP00000396135.1:n.-67G>A
ENST00000421141.5:c.-67G>A ENSP00000399981.1:n.-67G>A
ENST00000429896.6:c.-67G>A ENSP00000414823.2:n.-67G>A
ENST00000430669.6:c.189G>A ENSP00000410287.2:p.Trp63Ter
ENST00000437951.5:c.189G>A ENSP00000389744.1:p.Trp63Ter
ENST00000468211.6:c.189G>A ENSP00000449745.1:p.Trp63Ter
ENST00000546820.5:c.-67G>A ENSP00000448843.1:n.-67G>A
ENST00000547672.5:c.-67G>A ENSP00000447878.1:n.-67G>A
ENST00000548420.1:c.-102G>A ENSP00000449078.1:n.-102G>A
ENST00000548945.6:n.186G>A
ENST00000550914.6:c.-67G>A ENSP00000450047.1:n.-67G>A
ENST00000551425.1:n.190+10055G>A
ENST00000551623.1:c.36+10209G>A ENSP00000447242.1:n.36+10209G>A
ENST00000551630.1:c.-67G>A ENSP00000450131.1:n.-67G>A
ENST00000551845.5:c.-67G>A ENSP00000447008.1:n.-67G>A
ENST00000553011.5:c.-67G>A ENSP00000447797.1:n.-67G>A
ENST00000711046.1:c.189G>A ENSP00000518556.1:p.Trp63Ter
XM_011518868.1:c.387G>A XP_011517170.1:p.Trp129Ter
XM_011518871.1:c.-60+10055G>A XP_011517173.1:n.-60+10055G>A
XM_011518873.1:c.-102G>A XP_011517175.1:n.-102G>A
XM_011518874.1:c.387G>A XP_011517176.1:p.Trp129Ter