Canonical Allele Identifier: CA1953324076

Gene: PTH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13492487A= , CM000673.2:g.13492487A=	GRCh38
NC_000011.9:g.13514034A= , CM000673.1:g.13514034A=	GRCh37
NC_000011.8:g.13470610A=	NCBI36
NG_008962.1:g.8534T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000282091.6:c.266T= MANE Select	ENSP00000282091.1:p.Val89=
ENST00000282091.5:c.266T=	ENSP00000282091.1:p.Val89=
ENST00000529816.1:c.266T=	ENSP00000433208.1:p.Val89=
NM_000315.2:c.266T=	NP_000306.1:p.Val89=
NM_000315.3:c.266T=	NP_000306.1:p.Val89=
NM_001316352.1:c.362T=	NP_001303281.1:p.Val121=
NM_000315.4:c.266T= MANE Select	NP_000306.1:p.Val89=
NM_001316352.2:c.362T=	NP_001303281.1:p.Val121=