Canonical Allele Identifier: CA2419640786
Gene: PTCHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.23393500T= , CM000685.2:g.23393500T= GRCh38
NC_000023.10:g.23411617T= , CM000685.1:g.23411617T= GRCh37
NC_000023.9:g.23321538T= NCBI36
NG_021300.1:g.63633T=

Transcript Alleles

HGVS Amino-acid change
ENST00000379361.5:c.1982T= MANE Select ENSP00000368666.4:p.Leu661=
ENST00000379361.4:c.1982T= ENSP00000368666.4:p.Leu661=
NM_173495.2:c.1982T= NP_775766.2:p.Leu661=
XM_011545449.1:c.1982T= XP_011543751.1:p.Leu661=
XM_011545449.3:c.1982T= XP_011543751.1:p.Leu661=
NM_173495.3:c.1982T= MANE Select NP_775766.2:p.Leu661=