Canonical Allele Identifier: CA1846886908

Gene: GRHPR

Linked Data

• dbSNP Id: rs1823696517

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436938dup , CM000671.2:g.37436938dup	GRCh38
NC_000009.11:g.37436935dup , CM000671.1:g.37436935dup	GRCh37
NC_000009.10:g.37426935dup	NCBI36
NG_008135.1:g.19229dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*156dup MANE Select	ENSP00000313432.6:n.*156dup
ENST00000318158.10:c.*156dup	ENSP00000313432.6:n.*156dup
ENST00000480596.5:n.1844dup
ENST00000494290.1:c.*109dup	ENSP00000432021.1:n.*109dup
ENST00000497693.1:n.4711dup
NM_012203.1:c.*156dup	NP_036335.1:n.*156dup
XM_005251631.1:c.*156dup	XP_005251688.1:n.*156dup
XM_011518073.1:c.*156dup	XP_011516375.1:n.*156dup
XM_017015320.2:c.946-473dup	XP_016870809.1:n.946-473dup
XM_017015321.2:c.866-473dup	XP_016870810.1:n.866-473dup
XM_017015323.2:c.544-473dup	XP_016870812.1:n.544-473dup
XM_024447716.1:c.1219-473dup	XP_024303484.1:n.1219-473dup
XM_024447717.1:c.1139-473dup	XP_024303485.1:n.1139-473dup
XR_002956828.1:n.1234-473dup
XR_002956829.1:n.1154-473dup
XR_002956830.1:n.2563dup
XR_002956831.1:n.2238dup
XR_002956832.1:n.1562dup
NM_012203.2:c.*156dup MANE Select	NP_036335.1:n.*156dup