Canonical Allele Identifier: CA192896092

Gene: GRHPR

Linked Data

• dbSNP Id: rs781473642
• gnomAD v3: 9-37436431-ACATTGTGACTGGGTTTTAGTAGCCT-A
• gnomAD v4: 9-37436431-ACATTGTGACTGGGTTTTAGTAGCCT-A
• MyVariant Identifiers: chr9:g.37436429_37436453del (hg19) ; chr9:g.37436432_37436456del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436432_37436456del , CM000671.2:g.37436432_37436456del	GRCh38
NC_000009.11:g.37436429_37436453del , CM000671.1:g.37436429_37436453del	GRCh37
NC_000009.10:g.37426429_37426453del	NCBI36
NG_008135.1:g.18723_18747del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-229_866-205del MANE Select	ENSP00000313432.6:n.866-229_866-205del
ENST00000318158.10:c.866-229_866-205del	ENSP00000313432.6:n.866-229_866-205del
ENST00000460882.5:n.893-229_893-205del
ENST00000480596.5:n.1567-229_1567-205del
ENST00000491488.5:n.571-229_571-205del
ENST00000494290.1:c.*52-449_*52-425del	ENSP00000432021.1:n.*52-449_*52-425del
ENST00000497693.1:n.4434-229_4434-205del
NM_012203.1:c.866-229_866-205del	NP_036335.1:n.866-229_866-205del
XM_005251631.1:c.545-229_545-205del	XP_005251688.1:n.545-229_545-205del
XM_011518073.1:c.464-229_464-205del	XP_011516375.1:n.464-229_464-205del
XM_017015320.2:c.946-979_946-955del	XP_016870809.1:n.946-979_946-955del
XM_017015321.2:c.866-979_866-955del	XP_016870810.1:n.866-979_866-955del
XM_017015323.2:c.544-979_544-955del	XP_016870812.1:n.544-979_544-955del
XM_024447716.1:c.1219-979_1219-955del	XP_024303484.1:n.1219-979_1219-955del
XM_024447717.1:c.1139-979_1139-955del	XP_024303485.1:n.1139-979_1139-955del
XR_002956828.1:n.1234-979_1234-955del
XR_002956829.1:n.1154-979_1154-955del
XR_002956830.1:n.2286-229_2286-205del
XR_002956831.1:n.1961-229_1961-205del
XR_002956832.1:n.1285-229_1285-205del
NM_012203.2:c.866-229_866-205del MANE Select	NP_036335.1:n.866-229_866-205del