Canonical Allele Identifier: CA2689981211

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37429594-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429594T>G , CM000671.2:g.37429594T>G	GRCh38
NC_000009.11:g.37429591T>G , CM000671.1:g.37429591T>G	GRCh37
NC_000009.10:g.37419591T>G	NCBI36
NG_008135.1:g.11885T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.494-138T>G MANE Select	ENSP00000313432.6:n.494-138T>G
ENST00000318158.10:c.494-138T>G	ENSP00000313432.6:n.494-138T>G
ENST00000377824.8:n.531-138T>G
ENST00000460882.5:n.521-138T>G
ENST00000480596.5:n.1057T>G
ENST00000491488.5:n.199-138T>G
ENST00000494290.1:c.-74T>G	ENSP00000432021.1:n.-74T>G
ENST00000497693.1:n.1889T>G
ENST00000607784.1:c.494-138T>G	ENSP00000475569.1:n.494-138T>G
NM_012203.1:c.494-138T>G	NP_036335.1:n.494-138T>G
XM_005251631.1:c.173-138T>G	XP_005251688.1:n.173-138T>G
XM_011518073.1:c.92-138T>G	XP_011516375.1:n.92-138T>G
XR_929374.1:n.939-138T>G
XM_017015320.2:c.494-138T>G	XP_016870809.1:n.494-138T>G
XM_017015321.2:c.494-138T>G	XP_016870810.1:n.494-138T>G
XM_017015323.2:c.92-138T>G	XP_016870812.1:n.92-138T>G
XM_024447716.1:c.767-138T>G	XP_024303484.1:n.767-138T>G
XM_024447717.1:c.767-138T>G	XP_024303485.1:n.767-138T>G
XR_002956828.1:n.782-138T>G
XR_002956829.1:n.782-138T>G
XR_002956830.1:n.553-138T>G
XR_002956831.1:n.228-138T>G
XR_002956832.1:n.913-138T>G
NM_012203.2:c.494-138T>G MANE Select	NP_036335.1:n.494-138T>G