Canonical Allele Identifier: CA1953324103

Gene: PTH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13492498C= , CM000673.2:g.13492498C=	GRCh38
NC_000011.9:g.13514045C= , CM000673.1:g.13514045C=	GRCh37
NC_000011.8:g.13470621C=	NCBI36
NG_008962.1:g.8523G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000282091.6:c.255G= MANE Select	ENSP00000282091.1:p.Lys85=
ENST00000282091.5:c.255G=	ENSP00000282091.1:p.Lys85=
ENST00000529816.1:c.255G=	ENSP00000433208.1:p.Lys85=
NM_000315.2:c.255G=	NP_000306.1:p.Lys85=
NM_000315.3:c.255G=	NP_000306.1:p.Lys85=
NM_001316352.1:c.351G=	NP_001303281.1:p.Lys117=
NM_000315.4:c.255G= MANE Select	NP_000306.1:p.Lys85=
NM_001316352.2:c.351G=	NP_001303281.1:p.Lys117=