Canonical Allele Identifier: CA1846885309
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37436624C= , CM000671.2:g.37436624C= GRCh38
NC_000009.11:g.37436621C= , CM000671.1:g.37436621C= GRCh37
NC_000009.10:g.37426621C= NCBI36
NG_008135.1:g.18915C=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.866-37C= MANE Select ENSP00000313432.6:n.866-37C=
ENST00000318158.10:c.866-37C= ENSP00000313432.6:n.866-37C=
ENST00000460882.5:n.893-37C=
ENST00000480596.5:n.1567-37C=
ENST00000491488.5:n.571-37C=
ENST00000494290.1:c.*52-257C= ENSP00000432021.1:n.*52-257C=
ENST00000497693.1:n.4434-37C=
NM_012203.1:c.866-37C= NP_036335.1:n.866-37C=
XM_005251631.1:c.545-37C= XP_005251688.1:n.545-37C=
XM_011518073.1:c.464-37C= XP_011516375.1:n.464-37C=
XM_017015320.2:c.946-787C= XP_016870809.1:n.946-787C=
XM_017015321.2:c.866-787C= XP_016870810.1:n.866-787C=
XM_017015323.2:c.544-787C= XP_016870812.1:n.544-787C=
XM_024447716.1:c.1219-787C= XP_024303484.1:n.1219-787C=
XM_024447717.1:c.1139-787C= XP_024303485.1:n.1139-787C=
XR_002956828.1:n.1234-787C=
XR_002956829.1:n.1154-787C=
XR_002956830.1:n.2286-37C=
XR_002956831.1:n.1961-37C=
XR_002956832.1:n.1285-37C=
NM_012203.2:c.866-37C= MANE Select NP_036335.1:n.866-37C=