Canonical Allele Identifier: CA918449667

Gene: GRHPR

Linked Data

• dbSNP Id: rs34302950

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436639_37436652dup , CM000671.2:g.37436639_37436652dup	GRCh38
NC_000009.11:g.37436636_37436649dup , CM000671.1:g.37436636_37436649dup	GRCh37
NC_000009.10:g.37426636_37426649dup	NCBI36
NG_008135.1:g.18930_18943dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.866-22_866-9dup MANE Select	ENSP00000313432.6:n.866-22_866-9dup
ENST00000318158.10:c.866-22_866-9dup	ENSP00000313432.6:n.866-22_866-9dup
ENST00000460882.5:n.893-22_893-9dup
ENST00000480596.5:n.1567-22_1567-9dup
ENST00000491488.5:n.571-22_571-9dup
ENST00000494290.1:c.*52-242_*52-229dup	ENSP00000432021.1:n.*52-242_*52-229dup
ENST00000497693.1:n.4434-22_4434-9dup
NM_012203.1:c.866-22_866-9dup	NP_036335.1:n.866-22_866-9dup
XM_005251631.1:c.545-22_545-9dup	XP_005251688.1:n.545-22_545-9dup
XM_011518073.1:c.464-22_464-9dup	XP_011516375.1:n.464-22_464-9dup
XM_017015320.2:c.946-772_946-759dup	XP_016870809.1:n.946-772_946-759dup
XM_017015321.2:c.866-772_866-759dup	XP_016870810.1:n.866-772_866-759dup
XM_017015323.2:c.544-772_544-759dup	XP_016870812.1:n.544-772_544-759dup
XM_024447716.1:c.1219-772_1219-759dup	XP_024303484.1:n.1219-772_1219-759dup
XM_024447717.1:c.1139-772_1139-759dup	XP_024303485.1:n.1139-772_1139-759dup
XR_002956828.1:n.1234-772_1234-759dup
XR_002956829.1:n.1154-772_1154-759dup
XR_002956830.1:n.2286-22_2286-9dup
XR_002956831.1:n.1961-22_1961-9dup
XR_002956832.1:n.1285-22_1285-9dup
NM_012203.2:c.866-22_866-9dup MANE Select	NP_036335.1:n.866-22_866-9dup