Canonical Allele Identifier: CA2689984683

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436931-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436931G>A , CM000671.2:g.37436931G>A	GRCh38
NC_000009.11:g.37436928G>A , CM000671.1:g.37436928G>A	GRCh37
NC_000009.10:g.37426928G>A	NCBI36
NG_008135.1:g.19222G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*149G>A MANE Select	ENSP00000313432.6:n.*149G>A
ENST00000318158.10:c.*149G>A	ENSP00000313432.6:n.*149G>A
ENST00000480596.5:n.1837G>A
ENST00000494290.1:c.*102G>A	ENSP00000432021.1:n.*102G>A
ENST00000497693.1:n.4704G>A
NM_012203.1:c.*149G>A	NP_036335.1:n.*149G>A
XM_005251631.1:c.*149G>A	XP_005251688.1:n.*149G>A
XM_011518073.1:c.*149G>A	XP_011516375.1:n.*149G>A
XM_017015320.2:c.946-480G>A	XP_016870809.1:n.946-480G>A
XM_017015321.2:c.866-480G>A	XP_016870810.1:n.866-480G>A
XM_017015323.2:c.544-480G>A	XP_016870812.1:n.544-480G>A
XM_024447716.1:c.1219-480G>A	XP_024303484.1:n.1219-480G>A
XM_024447717.1:c.1139-480G>A	XP_024303485.1:n.1139-480G>A
XR_002956828.1:n.1234-480G>A
XR_002956829.1:n.1154-480G>A
XR_002956830.1:n.2556G>A
XR_002956831.1:n.2231G>A
XR_002956832.1:n.1555G>A
NM_012203.2:c.*149G>A MANE Select	NP_036335.1:n.*149G>A