Canonical Allele Identifier: CA1846887138

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436982T= , CM000671.2:g.37436982T=	GRCh38
NC_000009.11:g.37436979T= , CM000671.1:g.37436979T=	GRCh37
NC_000009.10:g.37426979T=	NCBI36
NG_008135.1:g.19273T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*200T= MANE Select	ENSP00000313432.6:n.*200T=
ENST00000318158.10:c.*200T=	ENSP00000313432.6:n.*200T=
ENST00000480596.5:n.1888T=
ENST00000494290.1:c.*153T=	ENSP00000432021.1:n.*153T=
ENST00000497693.1:n.4755T=
NM_012203.1:c.*200T=	NP_036335.1:n.*200T=
XM_005251631.1:c.*200T=	XP_005251688.1:n.*200T=
XM_011518073.1:c.*200T=	XP_011516375.1:n.*200T=
XM_017015320.2:c.946-429T=	XP_016870809.1:n.946-429T=
XM_017015321.2:c.866-429T=	XP_016870810.1:n.866-429T=
XM_017015323.2:c.544-429T=	XP_016870812.1:n.544-429T=
XM_024447716.1:c.1219-429T=	XP_024303484.1:n.1219-429T=
XM_024447717.1:c.1139-429T=	XP_024303485.1:n.1139-429T=
XR_002956828.1:n.1234-429T=
XR_002956829.1:n.1154-429T=
XR_002956830.1:n.2607T=
XR_002956831.1:n.2282T=
XR_002956832.1:n.1606T=
NM_012203.2:c.*200T= MANE Select	NP_036335.1:n.*200T=