Canonical Allele Identifier: CA1953324329

Gene: PTH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13492596C= , CM000673.2:g.13492596C=	GRCh38
NC_000011.9:g.13514143C= , CM000673.1:g.13514143C=	GRCh37
NC_000011.8:g.13470719C=	NCBI36
NG_008962.1:g.8425G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000282091.6:c.157G= MANE Select	ENSP00000282091.1:p.Glu53=
ENST00000282091.5:c.157G=	ENSP00000282091.1:p.Glu53=
ENST00000529816.1:c.157G=	ENSP00000433208.1:p.Glu53=
NM_000315.2:c.157G=	NP_000306.1:p.Glu53=
NM_000315.3:c.157G=	NP_000306.1:p.Glu53=
NM_001316352.1:c.253G=	NP_001303281.1:p.Glu85=
NM_000315.4:c.157G= MANE Select	NP_000306.1:p.Glu53=
NM_001316352.2:c.253G=	NP_001303281.1:p.Glu85=