Canonical Allele Identifier: CA1846885710
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37436709T= , CM000671.2:g.37436709T= GRCh38
NC_000009.11:g.37436706T= , CM000671.1:g.37436706T= GRCh37
NC_000009.10:g.37426706T= NCBI36
NG_008135.1:g.19000T=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.914T= MANE Select ENSP00000313432.6:p.Met305=
ENST00000318158.10:c.914T= ENSP00000313432.6:p.Met305=
ENST00000460882.5:n.941T=
ENST00000480596.5:n.1615T=
ENST00000494290.1:c.*52-172T= ENSP00000432021.1:n.*52-172T=
ENST00000497693.1:n.4482T=
NM_012203.1:c.914T= NP_036335.1:p.Met305=
XM_005251631.1:c.593T= XP_005251688.1:p.Met198=
XM_011518073.1:c.512T= XP_011516375.1:p.Met171=
XM_017015320.2:c.946-702T= XP_016870809.1:n.946-702T=
XM_017015321.2:c.866-702T= XP_016870810.1:n.866-702T=
XM_017015323.2:c.544-702T= XP_016870812.1:n.544-702T=
XM_024447716.1:c.1219-702T= XP_024303484.1:n.1219-702T=
XM_024447717.1:c.1139-702T= XP_024303485.1:n.1139-702T=
XR_002956828.1:n.1234-702T=
XR_002956829.1:n.1154-702T=
XR_002956830.1:n.2334T=
XR_002956831.1:n.2009T=
XR_002956832.1:n.1333T=
NM_012203.2:c.914T= MANE Select NP_036335.1:p.Met305=