Canonical Allele Identifier: CA1362309760
Gene: PTH1R HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000449590.6:c.395C= MANE Select ENSP00000402723.1:p.Pro132=
ENST00000313049.9:c.395C= ENSP00000321999.4:p.Pro132=
ENST00000418619.5:c.395C= ENSP00000411424.1:p.Pro132=
ENST00000427125.6:c.395C= ENSP00000400977.2:p.Pro132=
ENST00000428220.1:c.395C= ENSP00000389811.1:p.Pro132=
ENST00000430002.6:c.395C= ENSP00000413774.2:p.Pro132=
ENST00000449590.5:c.395C= ENSP00000402723.1:p.Pro132=
ENST00000490109.1:n.415C=
NM_000316.2:c.395C= NP_000307.1:p.Pro132=
NM_001184744.1:c.395C= NP_001171673.1:p.Pro132=
XM_005265344.2:c.302C= XP_005265401.1:p.Pro101=
XM_011533967.1:c.434C= XP_011532269.1:p.Pro145=
XM_011533968.1:c.416C= XP_011532270.1:p.Pro139=
XM_005265344.3:c.302C= XP_005265401.1:p.Pro101=
XM_011533967.3:c.434C= XP_011532269.1:p.Pro145=
XM_011533968.2:c.416C= XP_011532270.1:p.Pro139=
XM_017006932.2:c.434C= XP_016862421.1:p.Pro145=
XM_017006933.1:c.395C= XP_016862422.1:p.Pro132=
XM_017006934.1:c.434C= XP_016862423.1:p.Pro145=
NM_000316.3:c.395C= MANE Select NP_000307.1:p.Pro132=