Canonical Allele Identifier: CA863722903

Gene: GRHPR

Linked Data

• dbSNP Id: rs1400215940
• gnomAD v3: 9-37436461-GCCCTTCA-G
• gnomAD v4: 9-37436461-GCCCTTCA-G
• MyVariant Identifiers: chr9:g.37436459_37436465del (hg19) ; chr9:g.37436462_37436468del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436463_37436469del , CM000671.2:g.37436463_37436469del	GRCh38
NC_000009.11:g.37436460_37436466del , CM000671.1:g.37436460_37436466del	GRCh37
NC_000009.10:g.37426460_37426466del	NCBI36
NG_008135.1:g.18754_18760del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-198_866-192del MANE Select	ENSP00000313432.6:n.866-198_866-192del
ENST00000318158.10:c.866-198_866-192del	ENSP00000313432.6:n.866-198_866-192del
ENST00000460882.5:n.893-198_893-192del
ENST00000480596.5:n.1567-198_1567-192del
ENST00000491488.5:n.571-198_571-192del
ENST00000494290.1:c.*52-418_*52-412del	ENSP00000432021.1:n.*52-418_*52-412del
ENST00000497693.1:n.4434-198_4434-192del
NM_012203.1:c.866-198_866-192del	NP_036335.1:n.866-198_866-192del
XM_005251631.1:c.545-198_545-192del	XP_005251688.1:n.545-198_545-192del
XM_011518073.1:c.464-198_464-192del	XP_011516375.1:n.464-198_464-192del
XM_017015320.2:c.946-948_946-942del	XP_016870809.1:n.946-948_946-942del
XM_017015321.2:c.866-948_866-942del	XP_016870810.1:n.866-948_866-942del
XM_017015323.2:c.544-948_544-942del	XP_016870812.1:n.544-948_544-942del
XM_024447716.1:c.1219-948_1219-942del	XP_024303484.1:n.1219-948_1219-942del
XM_024447717.1:c.1139-948_1139-942del	XP_024303485.1:n.1139-948_1139-942del
XR_002956828.1:n.1234-948_1234-942del
XR_002956829.1:n.1154-948_1154-942del
XR_002956830.1:n.2286-198_2286-192del
XR_002956831.1:n.1961-198_1961-192del
XR_002956832.1:n.1285-198_1285-192del
NM_012203.2:c.866-198_866-192del MANE Select	NP_036335.1:n.866-198_866-192del