Canonical Allele Identifier: CA1846885832

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436750G= , CM000671.2:g.37436750G=	GRCh38
NC_000009.11:g.37436747G= , CM000671.1:g.37436747G=	GRCh37
NC_000009.10:g.37426747G=	NCBI36
NG_008135.1:g.19041G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.955G= MANE Select	ENSP00000313432.6:p.Gly319=
ENST00000318158.10:c.955G=	ENSP00000313432.6:p.Gly319=
ENST00000460882.5:n.982G=
ENST00000480596.5:n.1656G=
ENST00000494290.1:c.*52-131G=	ENSP00000432021.1:n.*52-131G=
ENST00000497693.1:n.4523G=
NM_012203.1:c.955G=	NP_036335.1:p.Gly319=
XM_005251631.1:c.634G=	XP_005251688.1:p.Gly212=
XM_011518073.1:c.553G=	XP_011516375.1:p.Gly185=
XM_017015320.2:c.946-661G=	XP_016870809.1:n.946-661G=
XM_017015321.2:c.866-661G=	XP_016870810.1:n.866-661G=
XM_017015323.2:c.544-661G=	XP_016870812.1:n.544-661G=
XM_024447716.1:c.1219-661G=	XP_024303484.1:n.1219-661G=
XM_024447717.1:c.1139-661G=	XP_024303485.1:n.1139-661G=
XR_002956828.1:n.1234-661G=
XR_002956829.1:n.1154-661G=
XR_002956830.1:n.2375G=
XR_002956831.1:n.2050G=
XR_002956832.1:n.1374G=
NM_012203.2:c.955G= MANE Select	NP_036335.1:p.Gly319=