Canonical Allele Identifier: CA863722975

Gene: GRHPR

Linked Data

• dbSNP Id: rs1464677564
• gnomAD v3: 9-37436563-ATTC-A
• gnomAD v4: 9-37436563-ATTC-A
• MyVariant Identifiers: chr9:g.37436561_37436563del (hg19) ; chr9:g.37436564_37436566del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436569_37436571del , CM000671.2:g.37436569_37436571del	GRCh38
NC_000009.11:g.37436566_37436568del , CM000671.1:g.37436566_37436568del	GRCh37
NC_000009.10:g.37426566_37426568del	NCBI36
NG_008135.1:g.18860_18862del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-92_866-90del MANE Select	ENSP00000313432.6:n.866-92_866-90del
ENST00000318158.10:c.866-92_866-90del	ENSP00000313432.6:n.866-92_866-90del
ENST00000460882.5:n.893-92_893-90del
ENST00000480596.5:n.1567-92_1567-90del
ENST00000491488.5:n.571-92_571-90del
ENST00000494290.1:c.*52-312_*52-310del	ENSP00000432021.1:n.*52-312_*52-310del
ENST00000497693.1:n.4434-92_4434-90del
NM_012203.1:c.866-92_866-90del	NP_036335.1:n.866-92_866-90del
XM_005251631.1:c.545-92_545-90del	XP_005251688.1:n.545-92_545-90del
XM_011518073.1:c.464-92_464-90del	XP_011516375.1:n.464-92_464-90del
XM_017015320.2:c.946-842_946-840del	XP_016870809.1:n.946-842_946-840del
XM_017015321.2:c.866-842_866-840del	XP_016870810.1:n.866-842_866-840del
XM_017015323.2:c.544-842_544-840del	XP_016870812.1:n.544-842_544-840del
XM_024447716.1:c.1219-842_1219-840del	XP_024303484.1:n.1219-842_1219-840del
XM_024447717.1:c.1139-842_1139-840del	XP_024303485.1:n.1139-842_1139-840del
XR_002956828.1:n.1234-842_1234-840del
XR_002956829.1:n.1154-842_1154-840del
XR_002956830.1:n.2286-92_2286-90del
XR_002956831.1:n.1961-92_1961-90del
XR_002956832.1:n.1285-92_1285-90del
NM_012203.2:c.866-92_866-90del MANE Select	NP_036335.1:n.866-92_866-90del