Canonical Allele Identifier: CA352494468

Gene: PTH1R

Linked Data

• MyVariant Identifiers: chr3:g.46939426C>A (hg19) ; chr3:g.46897936C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46897936C>A , CM000665.2:g.46897936C>A	GRCh38
NC_000003.11:g.46939426C>A , CM000665.1:g.46939426C>A	GRCh37
NC_000003.10:g.46914430C>A	NCBI36
NG_008864.1:g.25191C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000449590.6:c.395C>A MANE Select	ENSP00000402723.1:p.Pro132Gln
ENST00000313049.9:c.395C>A	ENSP00000321999.4:p.Pro132Gln
ENST00000418619.5:c.395C>A	ENSP00000411424.1:p.Pro132Gln
ENST00000427125.6:c.395C>A	ENSP00000400977.2:p.Pro132Gln
ENST00000428220.1:c.395C>A	ENSP00000389811.1:p.Pro132Gln
ENST00000430002.6:c.395C>A	ENSP00000413774.2:p.Pro132Gln
ENST00000449590.5:c.395C>A	ENSP00000402723.1:p.Pro132Gln
ENST00000490109.1:n.415C>A
NM_000316.2:c.395C>A	NP_000307.1:p.Pro132Gln
NM_001184744.1:c.395C>A	NP_001171673.1:p.Pro132Gln
XM_005265344.2:c.302C>A	XP_005265401.1:p.Pro101Gln
XM_011533967.1:c.434C>A	XP_011532269.1:p.Pro145Gln
XM_011533968.1:c.416C>A	XP_011532270.1:p.Pro139Gln
XM_005265344.3:c.302C>A	XP_005265401.1:p.Pro101Gln
XM_011533967.3:c.434C>A	XP_011532269.1:p.Pro145Gln
XM_011533968.2:c.416C>A	XP_011532270.1:p.Pro139Gln
XM_017006932.2:c.434C>A	XP_016862421.1:p.Pro145Gln
XM_017006933.1:c.395C>A	XP_016862422.1:p.Pro132Gln
XM_017006934.1:c.434C>A	XP_016862423.1:p.Pro145Gln
NM_000316.3:c.395C>A MANE Select	NP_000307.1:p.Pro132Gln