Canonical Allele Identifier: CA1846887134

Gene: GRHPR

Linked Data

• dbSNP Id: rs1823700920
• gnomAD v4: 9-37436981-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436985_37436986del , CM000671.2:g.37436985_37436986del	GRCh38
NC_000009.11:g.37436982_37436983del , CM000671.1:g.37436982_37436983del	GRCh37
NC_000009.10:g.37426982_37426983del	NCBI36
NG_008135.1:g.19276_19277del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*203_*204del MANE Select	ENSP00000313432.6:n.*203_*204del
ENST00000318158.10:c.*203_*204del	ENSP00000313432.6:n.*203_*204del
ENST00000480596.5:n.1891_1892del
ENST00000494290.1:c.*156_*157del	ENSP00000432021.1:n.*156_*157del
ENST00000497693.1:n.4758_4759del
NM_012203.1:c.*203_*204del	NP_036335.1:n.*203_*204del
XM_005251631.1:c.*203_*204del	XP_005251688.1:n.*203_*204del
XM_011518073.1:c.*203_*204del	XP_011516375.1:n.*203_*204del
XM_017015320.2:c.946-426_946-425del	XP_016870809.1:n.946-426_946-425del
XM_017015321.2:c.866-426_866-425del	XP_016870810.1:n.866-426_866-425del
XM_017015323.2:c.544-426_544-425del	XP_016870812.1:n.544-426_544-425del
XM_024447716.1:c.1219-426_1219-425del	XP_024303484.1:n.1219-426_1219-425del
XM_024447717.1:c.1139-426_1139-425del	XP_024303485.1:n.1139-426_1139-425del
XR_002956828.1:n.1234-426_1234-425del
XR_002956829.1:n.1154-426_1154-425del
XR_002956830.1:n.2610_2611del
XR_002956831.1:n.2285_2286del
XR_002956832.1:n.1609_1610del
NM_012203.2:c.*203_*204del MANE Select	NP_036335.1:n.*203_*204del