Canonical Allele Identifier: CA374115833
Community Standard Title: NM_000264.5(PTCH1):c.2017C>G (p.His673Asp)
Gene: PTCH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95468984G>C , CM000671.2:g.95468984G>C GRCh38
NC_000009.11:g.98231266G>C , CM000671.1:g.98231266G>C GRCh37
NC_000009.10:g.97271087G>C NCBI36
NG_007664.1:g.52982C>G , LRG_515:g.52982C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000264.5:c.2017C>G MANE Select NP_000255.2:p.His673Asp
ENST00000331920.11:c.2017C>G MANE Select ENSP00000332353.6:p.His673Asp
NM_001083603.3:c.2014C>G MANE Plus Clinical NP_001077072.1:p.His672Asp
ENST00000437951.6:c.2014C>G MANE Plus Clinical ENSP00000389744.2:p.His672Asp
NM_000264.3:c.2017C>G , LRG_515t1:c.2017C>G NP_000255.2:p.His673Asp
NM_000264.4:c.2017C>G NP_000255.2:p.His673Asp
NM_001083602.1:c.1819C>G , LRG_515t2:c.1819C>G NP_001077071.1:p.His607Asp
NM_001083602.2:c.1819C>G NP_001077071.1:p.His607Asp
NM_001083602.3:c.1819C>G NP_001077071.1:p.His607Asp
NM_001083603.1:c.2014C>G NP_001077072.1:p.His672Asp
NM_001083603.2:c.2014C>G NP_001077072.1:p.His672Asp
NM_001083604.1:c.1564C>G NP_001077073.1:p.His522Asp
NM_001083604.2:c.1564C>G NP_001077073.1:p.His522Asp
NM_001083604.3:c.1564C>G NP_001077073.1:p.His522Asp
NM_001083605.1:c.1564C>G NP_001077074.1:p.His522Asp
NM_001083605.2:c.1564C>G NP_001077074.1:p.His522Asp
NM_001083605.3:c.1564C>G NP_001077074.1:p.His522Asp
NM_001083606.1:c.1564C>G NP_001077075.1:p.His522Asp
NM_001083606.2:c.1564C>G NP_001077075.1:p.His522Asp
NM_001083606.3:c.1564C>G NP_001077075.1:p.His522Asp
NM_001083607.1:c.1564C>G NP_001077076.1:p.His522Asp
NM_001083607.2:c.1564C>G NP_001077076.1:p.His522Asp
NM_001083607.3:c.1564C>G NP_001077076.1:p.His522Asp
NM_001354918.1:c.1861C>G NP_001341847.1:p.His621Asp
NM_001354918.2:c.1861C>G NP_001341847.1:p.His621Asp
NR_038982.1:n.922G>C
NR_149061.1:n.2205C>G
NR_149061.2:n.2922C>G
ENST00000331920.10:c.2017C>G ENSP00000332353.6:p.His673Asp
ENST00000375271.4:c.1012C>G ENSP00000364420.4:p.His338Asp
ENST00000375274.6:c.2014C>G ENSP00000364423.2:p.His672Asp
ENST00000375290.6:c.1786C>G ENSP00000364439.2:n.1786C>G
ENST00000418258.5:c.1564C>G ENSP00000396135.1:p.His522Asp
ENST00000421141.5:c.1564C>G ENSP00000399981.1:p.His522Asp
ENST00000429896.6:c.1564C>G ENSP00000414823.2:p.His522Asp
ENST00000430669.6:c.1819C>G ENSP00000410287.2:p.His607Asp
ENST00000437951.5:c.1819C>G ENSP00000389744.1:p.His607Asp
ENST00000549678.1:n.206C>G
ENST00000690194.1:c.*325C>G ENSP00000509379.1:n.*325C>G
ENST00000692981.1:c.1564C>G ENSP00000510238.1:p.His522Asp
ENST00000711046.1:c.1819C>G ENSP00000518556.1:p.His607Asp
XM_005252102.2:c.1564C>G XP_005252159.1:p.His522Asp
XM_011518868.1:c.1861C>G XP_011517170.1:p.His621Asp
XM_011518869.1:c.1564C>G XP_011517171.1:p.His522Asp
XM_011518870.1:c.1564C>G XP_011517172.1:p.His522Asp
XM_011518871.1:c.1564C>G XP_011517173.1:p.His522Asp
XM_011518872.1:c.1564C>G XP_011517174.1:p.His522Asp
XM_011518873.1:c.1177C>G XP_011517175.1:p.His393Asp
XM_011518874.1:c.2017C>G XP_011517176.1:p.His673Asp