Canonical Allele Identifier: CA1846869115

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428556C= , CM000671.2:g.37428556C=	GRCh38
NC_000009.11:g.37428553C= , CM000671.1:g.37428553C=	GRCh37
NC_000009.10:g.37418553C=	NCBI36
NG_008135.1:g.10847C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.477C= MANE Select	ENSP00000313432.6:p.Ile159=
ENST00000318158.10:c.477C=	ENSP00000313432.6:p.Ile159=
ENST00000377824.8:n.514C=
ENST00000460882.5:n.504C=
ENST00000480596.5:n.19C=
ENST00000491488.5:n.182C=
ENST00000493368.5:n.534C=
ENST00000497693.1:n.851C=
ENST00000607784.1:c.477C=	ENSP00000475569.1:p.Ile159=
NM_012203.1:c.477C=	NP_036335.1:p.Ile159=
XM_005251631.1:c.156C=	XP_005251688.1:p.Ile52=
XM_011518073.1:c.-286C=	XP_011516375.1:n.-286C=
XR_929374.1:n.562C=
XM_017015320.2:c.477C=	XP_016870809.1:p.Ile159=
XM_017015321.2:c.477C=	XP_016870810.1:p.Ile159=
XM_017015323.2:c.-286C=	XP_016870812.1:n.-286C=
XM_024447716.1:c.750C=	XP_024303484.1:p.Ile250=
XM_024447717.1:c.750C=	XP_024303485.1:p.Ile250=
XR_002956828.1:n.765C=
XR_002956829.1:n.765C=
XR_002956830.1:n.536C=
XR_002956831.1:n.211C=
XR_002956832.1:n.536C=
NM_012203.2:c.477C= MANE Select	NP_036335.1:p.Ile159=