Canonical Allele Identifier: CA5059315

Gene: GRHPR

Linked Data

• dbSNP Id: rs767852031
• ExAC: 9:37436621 CTTCTT / C
• gnomAD v2: 9-37436621-CTTCTT-C
• gnomAD v3: 9-37436624-CTTCTT-C
• gnomAD v4: 9-37436624-CTTCTT-C
• MyVariant Identifiers: chr9:g.37436622_37436626del (hg19) ; chr9:g.37436625_37436629del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436625_37436629del , CM000671.2:g.37436625_37436629del	GRCh38
NC_000009.11:g.37436622_37436626del , CM000671.1:g.37436622_37436626del	GRCh37
NC_000009.10:g.37426622_37426626del	NCBI36
NG_008135.1:g.18916_18920del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.866-36_866-32del MANE Select	ENSP00000313432.6:n.866-36_866-32del
ENST00000318158.10:c.866-36_866-32del	ENSP00000313432.6:n.866-36_866-32del
ENST00000460882.5:n.893-36_893-32del
ENST00000480596.5:n.1567-36_1567-32del
ENST00000491488.5:n.571-36_571-32del
ENST00000494290.1:c.*52-256_*52-252del	ENSP00000432021.1:n.*52-256_*52-252del
ENST00000497693.1:n.4434-36_4434-32del
NM_012203.1:c.866-36_866-32del	NP_036335.1:n.866-36_866-32del
XM_005251631.1:c.545-36_545-32del	XP_005251688.1:n.545-36_545-32del
XM_011518073.1:c.464-36_464-32del	XP_011516375.1:n.464-36_464-32del
XM_017015320.2:c.946-786_946-782del	XP_016870809.1:n.946-786_946-782del
XM_017015321.2:c.866-786_866-782del	XP_016870810.1:n.866-786_866-782del
XM_017015323.2:c.544-786_544-782del	XP_016870812.1:n.544-786_544-782del
XM_024447716.1:c.1219-786_1219-782del	XP_024303484.1:n.1219-786_1219-782del
XM_024447717.1:c.1139-786_1139-782del	XP_024303485.1:n.1139-786_1139-782del
XR_002956828.1:n.1234-786_1234-782del
XR_002956829.1:n.1154-786_1154-782del
XR_002956830.1:n.2286-36_2286-32del
XR_002956831.1:n.1961-36_1961-32del
XR_002956832.1:n.1285-36_1285-32del
NM_012203.2:c.866-36_866-32del MANE Select	NP_036335.1:n.866-36_866-32del