Canonical Allele Identifier: CA2689984668

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436918-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436918T>A , CM000671.2:g.37436918T>A	GRCh38
NC_000009.11:g.37436915T>A , CM000671.1:g.37436915T>A	GRCh37
NC_000009.10:g.37426915T>A	NCBI36
NG_008135.1:g.19209T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*136T>A MANE Select	ENSP00000313432.6:n.*136T>A
ENST00000318158.10:c.*136T>A	ENSP00000313432.6:n.*136T>A
ENST00000480596.5:n.1824T>A
ENST00000494290.1:c.*89T>A	ENSP00000432021.1:n.*89T>A
ENST00000497693.1:n.4691T>A
NM_012203.1:c.*136T>A	NP_036335.1:n.*136T>A
XM_005251631.1:c.*136T>A	XP_005251688.1:n.*136T>A
XM_011518073.1:c.*136T>A	XP_011516375.1:n.*136T>A
XM_017015320.2:c.946-493T>A	XP_016870809.1:n.946-493T>A
XM_017015321.2:c.866-493T>A	XP_016870810.1:n.866-493T>A
XM_017015323.2:c.544-493T>A	XP_016870812.1:n.544-493T>A
XM_024447716.1:c.1219-493T>A	XP_024303484.1:n.1219-493T>A
XM_024447717.1:c.1139-493T>A	XP_024303485.1:n.1139-493T>A
XR_002956828.1:n.1234-493T>A
XR_002956829.1:n.1154-493T>A
XR_002956830.1:n.2543T>A
XR_002956831.1:n.2218T>A
XR_002956832.1:n.1542T>A
NM_012203.2:c.*136T>A MANE Select	NP_036335.1:n.*136T>A