Canonical Allele Identifier: CA1846885983

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436767T= , CM000671.2:g.37436767T=	GRCh38
NC_000009.11:g.37436764T= , CM000671.1:g.37436764T=	GRCh37
NC_000009.10:g.37426764T=	NCBI36
NG_008135.1:g.19058T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.972T= MANE Select	ENSP00000313432.6:p.Ser324=
ENST00000318158.10:c.972T=	ENSP00000313432.6:p.Ser324=
ENST00000460882.5:n.999T=
ENST00000480596.5:n.1673T=
ENST00000494290.1:c.*52-114T=	ENSP00000432021.1:n.*52-114T=
ENST00000497693.1:n.4540T=
NM_012203.1:c.972T=	NP_036335.1:p.Ser324=
XM_005251631.1:c.651T=	XP_005251688.1:p.Ser217=
XM_011518073.1:c.570T=	XP_011516375.1:p.Ser190=
XM_017015320.2:c.946-644T=	XP_016870809.1:n.946-644T=
XM_017015321.2:c.866-644T=	XP_016870810.1:n.866-644T=
XM_017015323.2:c.544-644T=	XP_016870812.1:n.544-644T=
XM_024447716.1:c.1219-644T=	XP_024303484.1:n.1219-644T=
XM_024447717.1:c.1139-644T=	XP_024303485.1:n.1139-644T=
XR_002956828.1:n.1234-644T=
XR_002956829.1:n.1154-644T=
XR_002956830.1:n.2392T=
XR_002956831.1:n.2067T=
XR_002956832.1:n.1391T=
NM_012203.2:c.972T= MANE Select	NP_036335.1:p.Ser324=