Canonical Allele Identifier: CA2689954916

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37428661-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428661C>A , CM000671.2:g.37428661C>A	GRCh38
NC_000009.11:g.37428658C>A , CM000671.1:g.37428658C>A	GRCh37
NC_000009.10:g.37418658C>A	NCBI36
NG_008135.1:g.10952C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.493+89C>A MANE Select	ENSP00000313432.6:n.493+89C>A
ENST00000318158.10:c.493+89C>A	ENSP00000313432.6:n.493+89C>A
ENST00000377824.8:n.530+89C>A
ENST00000460882.5:n.520+89C>A
ENST00000480596.5:n.124C>A
ENST00000491488.5:n.198+89C>A
ENST00000493368.5:n.639C>A
ENST00000497693.1:n.956C>A
ENST00000607784.1:c.493+89C>A	ENSP00000475569.1:n.493+89C>A
NM_012203.1:c.493+89C>A	NP_036335.1:n.493+89C>A
XM_005251631.1:c.172+89C>A	XP_005251688.1:n.172+89C>A
XM_011518073.1:c.-181C>A	XP_011516375.1:n.-181C>A
XR_929374.1:n.667C>A
XM_017015320.2:c.493+89C>A	XP_016870809.1:n.493+89C>A
XM_017015321.2:c.493+89C>A	XP_016870810.1:n.493+89C>A
XM_017015323.2:c.-181C>A	XP_016870812.1:n.-181C>A
XM_024447716.1:c.766+89C>A	XP_024303484.1:n.766+89C>A
XM_024447717.1:c.766+89C>A	XP_024303485.1:n.766+89C>A
XR_002956828.1:n.781+89C>A
XR_002956829.1:n.781+89C>A
XR_002956830.1:n.552+89C>A
XR_002956831.1:n.227+89C>A
XR_002956832.1:n.641C>A
NM_012203.2:c.493+89C>A MANE Select	NP_036335.1:n.493+89C>A