Canonical Allele Identifier: CA1846885854
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37436752G= , CM000671.2:g.37436752G= GRCh38
NC_000009.11:g.37436749G= , CM000671.1:g.37436749G= GRCh37
NC_000009.10:g.37426749G= NCBI36
NG_008135.1:g.19043G=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.957G= MANE Select ENSP00000313432.6:p.Gly319=
ENST00000318158.10:c.957G= ENSP00000313432.6:p.Gly319=
ENST00000460882.5:n.984G=
ENST00000480596.5:n.1658G=
ENST00000494290.1:c.*52-129G= ENSP00000432021.1:n.*52-129G=
ENST00000497693.1:n.4525G=
NM_012203.1:c.957G= NP_036335.1:p.Gly319=
XM_005251631.1:c.636G= XP_005251688.1:p.Gly212=
XM_011518073.1:c.555G= XP_011516375.1:p.Gly185=
XM_017015320.2:c.946-659G= XP_016870809.1:n.946-659G=
XM_017015321.2:c.866-659G= XP_016870810.1:n.866-659G=
XM_017015323.2:c.544-659G= XP_016870812.1:n.544-659G=
XM_024447716.1:c.1219-659G= XP_024303484.1:n.1219-659G=
XM_024447717.1:c.1139-659G= XP_024303485.1:n.1139-659G=
XR_002956828.1:n.1234-659G=
XR_002956829.1:n.1154-659G=
XR_002956830.1:n.2377G=
XR_002956831.1:n.2052G=
XR_002956832.1:n.1376G=
NM_012203.2:c.957G= MANE Select NP_036335.1:p.Gly319=