Canonical Allele Identifier: CA515620263

Gene: PTCHD1

Linked Data

• MyVariant Identifiers: chrX:g.23411606C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.23393489C>T , CM000685.2:g.23393489C>T	GRCh38
NC_000023.10:g.23411606C>T , CM000685.1:g.23411606C>T	GRCh37
NC_000023.9:g.23321527C>T	NCBI36
NG_021300.1:g.63622C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000379361.5:c.1971C>T MANE Select	ENSP00000368666.4:p.Asn657=
ENST00000379361.4:c.1971C>T	ENSP00000368666.4:p.Asn657=
NM_173495.2:c.1971C>T	NP_775766.2:p.Asn657=
XM_011545449.1:c.1971C>T	XP_011543751.1:p.Asn657=
XM_011545449.3:c.1971C>T	XP_011543751.1:p.Asn657=
NM_173495.3:c.1971C>T MANE Select	NP_775766.2:p.Asn657=