Canonical Allele Identifier: CA1846885907
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37436758G= , CM000671.2:g.37436758G= GRCh38
NC_000009.11:g.37436755G= , CM000671.1:g.37436755G= GRCh37
NC_000009.10:g.37426755G= NCBI36
NG_008135.1:g.19049G=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.963G= MANE Select ENSP00000313432.6:p.Pro321=
ENST00000318158.10:c.963G= ENSP00000313432.6:p.Pro321=
ENST00000460882.5:n.990G=
ENST00000480596.5:n.1664G=
ENST00000494290.1:c.*52-123G= ENSP00000432021.1:n.*52-123G=
ENST00000497693.1:n.4531G=
NM_012203.1:c.963G= NP_036335.1:p.Pro321=
XM_005251631.1:c.642G= XP_005251688.1:p.Pro214=
XM_011518073.1:c.561G= XP_011516375.1:p.Pro187=
XM_017015320.2:c.946-653G= XP_016870809.1:n.946-653G=
XM_017015321.2:c.866-653G= XP_016870810.1:n.866-653G=
XM_017015323.2:c.544-653G= XP_016870812.1:n.544-653G=
XM_024447716.1:c.1219-653G= XP_024303484.1:n.1219-653G=
XM_024447717.1:c.1139-653G= XP_024303485.1:n.1139-653G=
XR_002956828.1:n.1234-653G=
XR_002956829.1:n.1154-653G=
XR_002956830.1:n.2383G=
XR_002956831.1:n.2058G=
XR_002956832.1:n.1382G=
NM_012203.2:c.963G= MANE Select NP_036335.1:p.Pro321=