Canonical Allele Identifier: CA863755238

Gene: GRHPR

Linked Data

• dbSNP Id: rs1297225903
• gnomAD v3: 9-37422704-GGGCCAGCTTCTGTACTGCCA-G
• gnomAD v4: 9-37422704-GGGCCAGCTTCTGTACTGCCA-G
• MyVariant Identifiers: chr9:g.37422702_37422721del (hg19) ; chr9:g.37422705_37422724del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37422707_37422726del , CM000671.2:g.37422707_37422726del	GRCh38
NC_000009.11:g.37422704_37422723del , CM000671.1:g.37422704_37422723del	GRCh37
NC_000009.10:g.37412704_37412723del	NCBI36
NG_008135.1:g.4998_5017del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.-44_-25del MANE Select	ENSP00000313432.6:n.-44_-25del
ENST00000318158.10:c.-44_-25del	ENSP00000313432.6:n.-44_-25del
ENST00000460882.5:n.12_31del
ENST00000493368.5:n.42_61del
XM_005251631.1:c.-44_-25del	XP_005251688.1:n.-44_-25del
XR_929374.1:n.42_61del
XM_017015320.2:c.-44_-25del	XP_016870809.1:n.-44_-25del
XM_017015321.2:c.-44_-25del	XP_016870810.1:n.-44_-25del
XM_017015323.2:c.-806_-787del	XP_016870812.1:n.-806_-787del
XM_024447716.1:c.258_277del	XP_024303484.1:p.Gln87ProfsTer9
XM_024447717.1:c.258_277del	XP_024303485.1:p.Gln87ProfsTer9
XR_002956828.1:n.273_292del
XR_002956829.1:n.273_292del
XR_002956830.1:n.16_35del
XR_002956831.1:n.12_31del
XR_002956832.1:n.16_35del
NM_012203.2:c.-44_-25del MANE Select	NP_036335.1:n.-44_-25del