Canonical Allele Identifier: CA515620271
Gene: PTCHD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.23411612A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.23393495A>G , CM000685.2:g.23393495A>G GRCh38
NC_000023.10:g.23411612A>G , CM000685.1:g.23411612A>G GRCh37
NC_000023.9:g.23321533A>G NCBI36
NG_021300.1:g.63628A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379361.5:c.1977A>G MANE Select ENSP00000368666.4:p.Glu659=
ENST00000379361.4:c.1977A>G ENSP00000368666.4:p.Glu659=
NM_173495.2:c.1977A>G NP_775766.2:p.Glu659=
XM_011545449.1:c.1977A>G XP_011543751.1:p.Glu659=
XM_011545449.3:c.1977A>G XP_011543751.1:p.Glu659=
NM_173495.3:c.1977A>G MANE Select NP_775766.2:p.Glu659=
Search 100 bp 5'
Search 100 bp 3'