Canonical Allele Identifier: CA913157694

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37432118dup (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432121dup , CM000671.2:g.37432121dup	GRCh38
NC_000009.11:g.37432118dup , CM000671.1:g.37432118dup	GRCh37
NC_000009.10:g.37422118dup	NCBI36
NG_008135.1:g.14412dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.848dup MANE Select	ENSP00000313432.6:p.Thr284AspfsTer28
ENST00000318158.10:c.848dup	ENSP00000313432.6:p.Thr284AspfsTer28
ENST00000460882.5:n.875dup
ENST00000480596.5:n.1549dup
ENST00000482603.1:n.301dup
ENST00000491488.5:n.553dup
ENST00000494290.1:c.*51+970dup	ENSP00000432021.1:n.*51+970dup
ENST00000497693.1:n.4416dup
ENST00000512404.2:n.35dup
ENST00000607784.1:c.848dup	ENSP00000475569.1:p.Thr284AspfsTer?
NM_012203.1:c.848dup	NP_036335.1:p.Thr284AspfsTer28
XM_005251631.1:c.527dup	XP_005251688.1:p.Thr177AspfsTer28
XM_011518073.1:c.446dup	XP_011516375.1:p.Thr150AspfsTer28
XM_017015320.2:c.848dup	XP_016870809.1:p.Thr284AspfsTer6
XM_017015321.2:c.848dup	XP_016870810.1:p.Thr284AspfsTer6
XM_017015323.2:c.446dup	XP_016870812.1:p.Thr150AspfsTer6
XM_024447716.1:c.1121dup	XP_024303484.1:p.Thr375AspfsTer6
XM_024447717.1:c.1121dup	XP_024303485.1:p.Thr375AspfsTer6
XR_002956828.1:n.1136dup
XR_002956829.1:n.1136dup
XR_002956830.1:n.2268dup
XR_002956831.1:n.1943dup
XR_002956832.1:n.1267dup
NM_012203.2:c.848dup MANE Select	NP_036335.1:p.Thr284AspfsTer28