Canonical Allele Identifier: CA1846885459

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436643T= , CM000671.2:g.37436643T=	GRCh38
NC_000009.11:g.37436640T= , CM000671.1:g.37436640T=	GRCh37
NC_000009.10:g.37426640T=	NCBI36
NG_008135.1:g.18934T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-18T= MANE Select	ENSP00000313432.6:n.866-18T=
ENST00000318158.10:c.866-18T=	ENSP00000313432.6:n.866-18T=
ENST00000460882.5:n.893-18T=
ENST00000480596.5:n.1567-18T=
ENST00000491488.5:n.571-18T=
ENST00000494290.1:c.*52-238T=	ENSP00000432021.1:n.*52-238T=
ENST00000497693.1:n.4434-18T=
NM_012203.1:c.866-18T=	NP_036335.1:n.866-18T=
XM_005251631.1:c.545-18T=	XP_005251688.1:n.545-18T=
XM_011518073.1:c.464-18T=	XP_011516375.1:n.464-18T=
XM_017015320.2:c.946-768T=	XP_016870809.1:n.946-768T=
XM_017015321.2:c.866-768T=	XP_016870810.1:n.866-768T=
XM_017015323.2:c.544-768T=	XP_016870812.1:n.544-768T=
XM_024447716.1:c.1219-768T=	XP_024303484.1:n.1219-768T=
XM_024447717.1:c.1139-768T=	XP_024303485.1:n.1139-768T=
XR_002956828.1:n.1234-768T=
XR_002956829.1:n.1154-768T=
XR_002956830.1:n.2286-18T=
XR_002956831.1:n.1961-18T=
XR_002956832.1:n.1285-18T=
NM_012203.2:c.866-18T= MANE Select	NP_036335.1:n.866-18T=