Canonical Allele Identifier: CA1123330207

Gene: GRHPR

Linked Data

• gnomAD v3: 9-37436653-C-CT
• gnomAD v4: 9-37436653-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436656dup , CM000671.2:g.37436656dup	GRCh38
NC_000009.11:g.37436653dup , CM000671.1:g.37436653dup	GRCh37
NC_000009.10:g.37426653dup	NCBI36
NG_008135.1:g.18947dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-5dup MANE Select	ENSP00000313432.6:n.866-5dup
ENST00000318158.10:c.866-5dup	ENSP00000313432.6:n.866-5dup
ENST00000460882.5:n.893-5dup
ENST00000480596.5:n.1567-5dup
ENST00000491488.5:n.571-5dup
ENST00000494290.1:c.*52-225dup	ENSP00000432021.1:n.*52-225dup
ENST00000497693.1:n.4434-5dup
NM_012203.1:c.866-5dup	NP_036335.1:n.866-5dup
XM_005251631.1:c.545-5dup	XP_005251688.1:n.545-5dup
XM_011518073.1:c.464-5dup	XP_011516375.1:n.464-5dup
XM_017015320.2:c.946-755dup	XP_016870809.1:n.946-755dup
XM_017015321.2:c.866-755dup	XP_016870810.1:n.866-755dup
XM_017015323.2:c.544-755dup	XP_016870812.1:n.544-755dup
XM_024447716.1:c.1219-755dup	XP_024303484.1:n.1219-755dup
XM_024447717.1:c.1139-755dup	XP_024303485.1:n.1139-755dup
XR_002956828.1:n.1234-755dup
XR_002956829.1:n.1154-755dup
XR_002956830.1:n.2286-5dup
XR_002956831.1:n.1961-5dup
XR_002956832.1:n.1285-5dup
NM_012203.2:c.866-5dup MANE Select	NP_036335.1:n.866-5dup