Canonical Allele Identifier: CA2579340799

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436813-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436813A>C , CM000671.2:g.37436813A>C	GRCh38
NC_000009.11:g.37436810A>C , CM000671.1:g.37436810A>C	GRCh37
NC_000009.10:g.37426810A>C	NCBI36
NG_008135.1:g.19104A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*31A>C MANE Select	ENSP00000313432.6:n.*31A>C
ENST00000318158.10:c.*31A>C	ENSP00000313432.6:n.*31A>C
ENST00000460882.5:n.1045A>C
ENST00000480596.5:n.1719A>C
ENST00000494290.1:c.*52-68A>C	ENSP00000432021.1:n.*52-68A>C
ENST00000497693.1:n.4586A>C
NM_012203.1:c.*31A>C	NP_036335.1:n.*31A>C
XM_005251631.1:c.*31A>C	XP_005251688.1:n.*31A>C
XM_011518073.1:c.*31A>C	XP_011516375.1:n.*31A>C
XM_017015320.2:c.946-598A>C	XP_016870809.1:n.946-598A>C
XM_017015321.2:c.866-598A>C	XP_016870810.1:n.866-598A>C
XM_017015323.2:c.544-598A>C	XP_016870812.1:n.544-598A>C
XM_024447716.1:c.1219-598A>C	XP_024303484.1:n.1219-598A>C
XM_024447717.1:c.1139-598A>C	XP_024303485.1:n.1139-598A>C
XR_002956828.1:n.1234-598A>C
XR_002956829.1:n.1154-598A>C
XR_002956830.1:n.2438A>C
XR_002956831.1:n.2113A>C
XR_002956832.1:n.1437A>C
NM_012203.2:c.*31A>C MANE Select	NP_036335.1:n.*31A>C