Canonical Allele Identifier: CA387002463
Gene: HPD HGNC NCBI
TIALD HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.122295327G>C (hg19) chr12:g.121857421G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121857421G>C , CM000674.2:g.121857421G>C GRCh38
NC_000012.11:g.122295327G>C , CM000674.1:g.122295327G>C GRCh37
NC_000012.10:g.120779710G>C NCBI36
NG_016461.1:g.36191C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289004.8:c.105C>G (HPD) MANE Select ENSP00000289004.4:p.Phe35Leu
ENST00000535114.1:n.461C>G (HPD)
ENST00000542159.2:n.163C>G (HPD)
ENST00000543163.5:c.-13C>G (HPD) ENSP00000441677.1:n.-13C>G
NM_001171993.1:c.-13C>G (HPD) NP_001165464.1:n.-13C>G
NM_002150.2:c.105C>G (HPD) NP_002141.1:p.Phe35Leu
XR_002957437.1:n.324-198G>C (TIALD)
NM_002150.3:c.105C>G (HPD) MANE Select NP_002141.2:p.Phe35Leu
NM_001171993.2:c.-13C>G (HPD) NP_001165464.1:n.-13C>G
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