Canonical Allele Identifier: CA387001948
Gene: HPD HGNC NCBI
TIALD HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.122295250A>T (hg19) chr12:g.121857344A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121857344A>T , CM000674.2:g.121857344A>T GRCh38
NC_000012.11:g.122295250A>T , CM000674.1:g.122295250A>T GRCh37
NC_000012.10:g.120779633A>T NCBI36
NG_016461.1:g.36268T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289004.8:c.182T>A (HPD) MANE Select ENSP00000289004.4:p.Val61Glu
ENST00000535114.1:n.538T>A (HPD)
ENST00000542159.2:n.240T>A (HPD)
ENST00000543163.5:c.65T>A (HPD) ENSP00000441677.1:p.Val22Glu
NM_001171993.1:c.65T>A (HPD) NP_001165464.1:p.Val22Glu
NM_002150.2:c.182T>A (HPD) NP_002141.1:p.Val61Glu
XR_002957437.1:n.324-275A>T (TIALD)
NM_002150.3:c.182T>A (HPD) MANE Select NP_002141.2:p.Val61Glu
NM_001171993.2:c.65T>A (HPD) NP_001165464.1:p.Val22Glu
Search 100 bp 5'
Search 100 bp 3'