Canonical Allele Identifier: CA433469061

Gene: PTH1R

Linked Data

• MyVariant Identifiers: chr3:g.46939418G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46897928G>A , CM000665.2:g.46897928G>A	GRCh38
NC_000003.11:g.46939418G>A , CM000665.1:g.46939418G>A	GRCh37
NC_000003.10:g.46914422G>A	NCBI36
NG_008864.1:g.25183G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000449590.6:c.387G>A MANE Select	ENSP00000402723.1:p.Val129=
ENST00000313049.9:c.387G>A	ENSP00000321999.4:p.Val129=
ENST00000418619.5:c.387G>A	ENSP00000411424.1:p.Val129=
ENST00000427125.6:c.387G>A	ENSP00000400977.2:p.Val129=
ENST00000428220.1:c.387G>A	ENSP00000389811.1:p.Val129=
ENST00000430002.6:c.387G>A	ENSP00000413774.2:p.Val129=
ENST00000449590.5:c.387G>A	ENSP00000402723.1:p.Val129=
ENST00000490109.1:n.407G>A
NM_000316.2:c.387G>A	NP_000307.1:p.Val129=
NM_001184744.1:c.387G>A	NP_001171673.1:p.Val129=
XM_005265344.2:c.294G>A	XP_005265401.1:p.Val98=
XM_011533967.1:c.426G>A	XP_011532269.1:p.Val142=
XM_011533968.1:c.408G>A	XP_011532270.1:p.Val136=
XM_005265344.3:c.294G>A	XP_005265401.1:p.Val98=
XM_011533967.3:c.426G>A	XP_011532269.1:p.Val142=
XM_011533968.2:c.408G>A	XP_011532270.1:p.Val136=
XM_017006932.2:c.426G>A	XP_016862421.1:p.Val142=
XM_017006933.1:c.387G>A	XP_016862422.1:p.Val129=
XM_017006934.1:c.426G>A	XP_016862423.1:p.Val142=
NM_000316.3:c.387G>A MANE Select	NP_000307.1:p.Val129=