Canonical Allele Identifier: CA2689984583

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436638-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436639del , CM000671.2:g.37436639del	GRCh38
NC_000009.11:g.37436636del , CM000671.1:g.37436636del	GRCh37
NC_000009.10:g.37426636del	NCBI36
NG_008135.1:g.18930del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-22del MANE Select	ENSP00000313432.6:n.866-22del
ENST00000318158.10:c.866-22del	ENSP00000313432.6:n.866-22del
ENST00000460882.5:n.893-22del
ENST00000480596.5:n.1567-22del
ENST00000491488.5:n.571-22del
ENST00000494290.1:c.*52-242del	ENSP00000432021.1:n.*52-242del
ENST00000497693.1:n.4434-22del
NM_012203.1:c.866-22del	NP_036335.1:n.866-22del
XM_005251631.1:c.545-22del	XP_005251688.1:n.545-22del
XM_011518073.1:c.464-22del	XP_011516375.1:n.464-22del
XM_017015320.2:c.946-772del	XP_016870809.1:n.946-772del
XM_017015321.2:c.866-772del	XP_016870810.1:n.866-772del
XM_017015323.2:c.544-772del	XP_016870812.1:n.544-772del
XM_024447716.1:c.1219-772del	XP_024303484.1:n.1219-772del
XM_024447717.1:c.1139-772del	XP_024303485.1:n.1139-772del
XR_002956828.1:n.1234-772del
XR_002956829.1:n.1154-772del
XR_002956830.1:n.2286-22del
XR_002956831.1:n.1961-22del
XR_002956832.1:n.1285-22del
NM_012203.2:c.866-22del MANE Select	NP_036335.1:n.866-22del