Canonical Allele Identifier: CA2689984622

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436844-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436844A>C , CM000671.2:g.37436844A>C	GRCh38
NC_000009.11:g.37436841A>C , CM000671.1:g.37436841A>C	GRCh37
NC_000009.10:g.37426841A>C	NCBI36
NG_008135.1:g.19135A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*62A>C MANE Select	ENSP00000313432.6:n.*62A>C
ENST00000318158.10:c.*62A>C	ENSP00000313432.6:n.*62A>C
ENST00000460882.5:n.1076A>C
ENST00000480596.5:n.1750A>C
ENST00000494290.1:c.*52-37A>C	ENSP00000432021.1:n.*52-37A>C
ENST00000497693.1:n.4617A>C
NM_012203.1:c.*62A>C	NP_036335.1:n.*62A>C
XM_005251631.1:c.*62A>C	XP_005251688.1:n.*62A>C
XM_011518073.1:c.*62A>C	XP_011516375.1:n.*62A>C
XM_017015320.2:c.946-567A>C	XP_016870809.1:n.946-567A>C
XM_017015321.2:c.866-567A>C	XP_016870810.1:n.866-567A>C
XM_017015323.2:c.544-567A>C	XP_016870812.1:n.544-567A>C
XM_024447716.1:c.1219-567A>C	XP_024303484.1:n.1219-567A>C
XM_024447717.1:c.1139-567A>C	XP_024303485.1:n.1139-567A>C
XR_002956828.1:n.1234-567A>C
XR_002956829.1:n.1154-567A>C
XR_002956830.1:n.2469A>C
XR_002956831.1:n.2144A>C
XR_002956832.1:n.1468A>C
NM_012203.2:c.*62A>C MANE Select	NP_036335.1:n.*62A>C