Canonical Allele Identifier: CA587805436

Gene: GRHPR

Linked Data

• dbSNP Id: rs1564305177
• gnomAD v2: 9-37436397-GCGCCCAGCC-G
• gnomAD v3: 9-37436400-GCGCCCAGCC-G
• gnomAD v4: 9-37436400-GCGCCCAGCC-G
• MyVariant Identifiers: chr9:g.37436398_37436406del (hg19) ; chr9:g.37436401_37436409del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436402_37436410del , CM000671.2:g.37436402_37436410del	GRCh38
NC_000009.11:g.37436399_37436407del , CM000671.1:g.37436399_37436407del	GRCh37
NC_000009.10:g.37426399_37426407del	NCBI36
NG_008135.1:g.18693_18701del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-259_866-251del MANE Select	ENSP00000313432.6:n.866-259_866-251del
ENST00000318158.10:c.866-259_866-251del	ENSP00000313432.6:n.866-259_866-251del
ENST00000460882.5:n.893-259_893-251del
ENST00000480596.5:n.1567-259_1567-251del
ENST00000491488.5:n.571-259_571-251del
ENST00000494290.1:c.*52-479_*52-471del	ENSP00000432021.1:n.*52-479_*52-471del
ENST00000497693.1:n.4434-259_4434-251del
NM_012203.1:c.866-259_866-251del	NP_036335.1:n.866-259_866-251del
XM_005251631.1:c.545-259_545-251del	XP_005251688.1:n.545-259_545-251del
XM_011518073.1:c.464-259_464-251del	XP_011516375.1:n.464-259_464-251del
XM_017015320.2:c.946-1009_946-1001del	XP_016870809.1:n.946-1009_946-1001del
XM_017015321.2:c.866-1009_866-1001del	XP_016870810.1:n.866-1009_866-1001del
XM_017015323.2:c.544-1009_544-1001del	XP_016870812.1:n.544-1009_544-1001del
XM_024447716.1:c.1219-1009_1219-1001del	XP_024303484.1:n.1219-1009_1219-1001del
XM_024447717.1:c.1139-1009_1139-1001del	XP_024303485.1:n.1139-1009_1139-1001del
XR_002956828.1:n.1234-1009_1234-1001del
XR_002956829.1:n.1154-1009_1154-1001del
XR_002956830.1:n.2286-259_2286-251del
XR_002956831.1:n.1961-259_1961-251del
XR_002956832.1:n.1285-259_1285-251del
NM_012203.2:c.866-259_866-251del MANE Select	NP_036335.1:n.866-259_866-251del