Canonical Allele Identifier: CA1846887014

Gene: GRHPR

Linked Data

• dbSNP Id: rs1823698243

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436954_37436958dup , CM000671.2:g.37436954_37436958dup	GRCh38
NC_000009.11:g.37436951_37436955dup , CM000671.1:g.37436951_37436955dup	GRCh37
NC_000009.10:g.37426951_37426955dup	NCBI36
NG_008135.1:g.19245_19249dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*172_*176dup MANE Select	ENSP00000313432.6:n.*172_*176dup
ENST00000318158.10:c.*172_*176dup	ENSP00000313432.6:n.*172_*176dup
ENST00000480596.5:n.1860_1864dup
ENST00000494290.1:c.*125_*129dup	ENSP00000432021.1:n.*125_*129dup
ENST00000497693.1:n.4727_4731dup
NM_012203.1:c.*172_*176dup	NP_036335.1:n.*172_*176dup
XM_005251631.1:c.*172_*176dup	XP_005251688.1:n.*172_*176dup
XM_011518073.1:c.*172_*176dup	XP_011516375.1:n.*172_*176dup
XM_017015320.2:c.946-457_946-453dup	XP_016870809.1:n.946-457_946-453dup
XM_017015321.2:c.866-457_866-453dup	XP_016870810.1:n.866-457_866-453dup
XM_017015323.2:c.544-457_544-453dup	XP_016870812.1:n.544-457_544-453dup
XM_024447716.1:c.1219-457_1219-453dup	XP_024303484.1:n.1219-457_1219-453dup
XM_024447717.1:c.1139-457_1139-453dup	XP_024303485.1:n.1139-457_1139-453dup
XR_002956828.1:n.1234-457_1234-453dup
XR_002956829.1:n.1154-457_1154-453dup
XR_002956830.1:n.2579_2583dup
XR_002956831.1:n.2254_2258dup
XR_002956832.1:n.1578_1582dup
NM_012203.2:c.*172_*176dup MANE Select	NP_036335.1:n.*172_*176dup