Canonical Allele Identifier: CA379724501
Gene: PTH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13492492G>T , CM000673.2:g.13492492G>T GRCh38
NC_000011.9:g.13514039G>T , CM000673.1:g.13514039G>T GRCh37
NC_000011.8:g.13470615G>T NCBI36
NG_008962.1:g.8529C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000282091.6:c.261C>A MANE Select ENSP00000282091.1:p.Asp87Glu
ENST00000282091.5:c.261C>A ENSP00000282091.1:p.Asp87Glu
ENST00000529816.1:c.261C>A ENSP00000433208.1:p.Asp87Glu
NM_000315.2:c.261C>A NP_000306.1:p.Asp87Glu
NM_000315.3:c.261C>A NP_000306.1:p.Asp87Glu
NM_001316352.1:c.357C>A NP_001303281.1:p.Asp119Glu
NM_000315.4:c.261C>A MANE Select NP_000306.1:p.Asp87Glu
NM_001316352.2:c.357C>A NP_001303281.1:p.Asp119Glu