Canonical Allele Identifier: CA1846885442

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436639T= , CM000671.2:g.37436639T=	GRCh38
NC_000009.11:g.37436636T= , CM000671.1:g.37436636T=	GRCh37
NC_000009.10:g.37426636T=	NCBI36
NG_008135.1:g.18930T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-22T= MANE Select	ENSP00000313432.6:n.866-22T=
ENST00000318158.10:c.866-22T=	ENSP00000313432.6:n.866-22T=
ENST00000460882.5:n.893-22T=
ENST00000480596.5:n.1567-22T=
ENST00000491488.5:n.571-22T=
ENST00000494290.1:c.*52-242T=	ENSP00000432021.1:n.*52-242T=
ENST00000497693.1:n.4434-22T=
NM_012203.1:c.866-22T=	NP_036335.1:n.866-22T=
XM_005251631.1:c.545-22T=	XP_005251688.1:n.545-22T=
XM_011518073.1:c.464-22T=	XP_011516375.1:n.464-22T=
XM_017015320.2:c.946-772T=	XP_016870809.1:n.946-772T=
XM_017015321.2:c.866-772T=	XP_016870810.1:n.866-772T=
XM_017015323.2:c.544-772T=	XP_016870812.1:n.544-772T=
XM_024447716.1:c.1219-772T=	XP_024303484.1:n.1219-772T=
XM_024447717.1:c.1139-772T=	XP_024303485.1:n.1139-772T=
XR_002956828.1:n.1234-772T=
XR_002956829.1:n.1154-772T=
XR_002956830.1:n.2286-22T=
XR_002956831.1:n.1961-22T=
XR_002956832.1:n.1285-22T=
NM_012203.2:c.866-22T= MANE Select	NP_036335.1:n.866-22T=