Canonical Allele Identifier: CA2689955011

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37428766-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428766T>A , CM000671.2:g.37428766T>A	GRCh38
NC_000009.11:g.37428763T>A , CM000671.1:g.37428763T>A	GRCh37
NC_000009.10:g.37418763T>A	NCBI36
NG_008135.1:g.11057T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.493+194T>A MANE Select	ENSP00000313432.6:n.493+194T>A
ENST00000318158.10:c.493+194T>A	ENSP00000313432.6:n.493+194T>A
ENST00000377824.8:n.530+194T>A
ENST00000460882.5:n.520+194T>A
ENST00000480596.5:n.229T>A
ENST00000491488.5:n.198+194T>A
ENST00000493368.5:n.744T>A
ENST00000497693.1:n.1061T>A
ENST00000607784.1:c.493+194T>A	ENSP00000475569.1:n.493+194T>A
NM_012203.1:c.493+194T>A	NP_036335.1:n.493+194T>A
XM_005251631.1:c.172+194T>A	XP_005251688.1:n.172+194T>A
XM_011518073.1:c.-76T>A	XP_011516375.1:n.-76T>A
XR_929374.1:n.772T>A
XM_017015320.2:c.493+194T>A	XP_016870809.1:n.493+194T>A
XM_017015321.2:c.493+194T>A	XP_016870810.1:n.493+194T>A
XM_017015323.2:c.-76T>A	XP_016870812.1:n.-76T>A
XM_024447716.1:c.766+194T>A	XP_024303484.1:n.766+194T>A
XM_024447717.1:c.766+194T>A	XP_024303485.1:n.766+194T>A
XR_002956828.1:n.781+194T>A
XR_002956829.1:n.781+194T>A
XR_002956830.1:n.552+194T>A
XR_002956831.1:n.227+194T>A
XR_002956832.1:n.746T>A
NM_012203.2:c.493+194T>A MANE Select	NP_036335.1:n.493+194T>A