Canonical Allele Identifier: CA1362309752

Gene: PTH1R

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46897935C= , CM000665.2:g.46897935C=	GRCh38
NC_000003.11:g.46939425C= , CM000665.1:g.46939425C=	GRCh37
NC_000003.10:g.46914429C=	NCBI36
NG_008864.1:g.25190C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449590.6:c.394C= MANE Select	ENSP00000402723.1:p.Pro132=
ENST00000313049.9:c.394C=	ENSP00000321999.4:p.Pro132=
ENST00000418619.5:c.394C=	ENSP00000411424.1:p.Pro132=
ENST00000427125.6:c.394C=	ENSP00000400977.2:p.Pro132=
ENST00000428220.1:c.394C=	ENSP00000389811.1:p.Pro132=
ENST00000430002.6:c.394C=	ENSP00000413774.2:p.Pro132=
ENST00000449590.5:c.394C=	ENSP00000402723.1:p.Pro132=
ENST00000490109.1:n.414C=
NM_000316.2:c.394C=	NP_000307.1:p.Pro132=
NM_001184744.1:c.394C=	NP_001171673.1:p.Pro132=
XM_005265344.2:c.301C=	XP_005265401.1:p.Pro101=
XM_011533967.1:c.433C=	XP_011532269.1:p.Pro145=
XM_011533968.1:c.415C=	XP_011532270.1:p.Pro139=
XM_005265344.3:c.301C=	XP_005265401.1:p.Pro101=
XM_011533967.3:c.433C=	XP_011532269.1:p.Pro145=
XM_011533968.2:c.415C=	XP_011532270.1:p.Pro139=
XM_017006932.2:c.433C=	XP_016862421.1:p.Pro145=
XM_017006933.1:c.394C=	XP_016862422.1:p.Pro132=
XM_017006934.1:c.433C=	XP_016862423.1:p.Pro145=
NM_000316.3:c.394C= MANE Select	NP_000307.1:p.Pro132=