Canonical Allele Identifier: CA1362309737
Gene: PTH1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46897924C= , CM000665.2:g.46897924C= GRCh38
NC_000003.11:g.46939414C= , CM000665.1:g.46939414C= GRCh37
NC_000003.10:g.46914418C= NCBI36
NG_008864.1:g.25179C=

Transcript Alleles

HGVS Amino-acid change
ENST00000449590.6:c.383C= MANE Select ENSP00000402723.1:p.Ala128=
ENST00000313049.9:c.383C= ENSP00000321999.4:p.Ala128=
ENST00000418619.5:c.383C= ENSP00000411424.1:p.Ala128=
ENST00000427125.6:c.383C= ENSP00000400977.2:p.Ala128=
ENST00000428220.1:c.383C= ENSP00000389811.1:p.Ala128=
ENST00000430002.6:c.383C= ENSP00000413774.2:p.Ala128=
ENST00000449590.5:c.383C= ENSP00000402723.1:p.Ala128=
ENST00000490109.1:n.403C=
NM_000316.2:c.383C= NP_000307.1:p.Ala128=
NM_001184744.1:c.383C= NP_001171673.1:p.Ala128=
XM_005265344.2:c.290C= XP_005265401.1:p.Ala97=
XM_011533967.1:c.422C= XP_011532269.1:p.Ala141=
XM_011533968.1:c.404C= XP_011532270.1:p.Ala135=
XM_005265344.3:c.290C= XP_005265401.1:p.Ala97=
XM_011533967.3:c.422C= XP_011532269.1:p.Ala141=
XM_011533968.2:c.404C= XP_011532270.1:p.Ala135=
XM_017006932.2:c.422C= XP_016862421.1:p.Ala141=
XM_017006933.1:c.383C= XP_016862422.1:p.Ala128=
XM_017006934.1:c.422C= XP_016862423.1:p.Ala141=
NM_000316.3:c.383C= MANE Select NP_000307.1:p.Ala128=