Canonical Allele Identifier: CA2689982925

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37432289-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432289T>A , CM000671.2:g.37432289T>A	GRCh38
NC_000009.11:g.37432286T>A , CM000671.1:g.37432286T>A	GRCh37
NC_000009.10:g.37422286T>A	NCBI36
NG_008135.1:g.14580T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.865+151T>A MANE Select	ENSP00000313432.6:n.865+151T>A
ENST00000318158.10:c.865+151T>A	ENSP00000313432.6:n.865+151T>A
ENST00000460882.5:n.892+151T>A
ENST00000480596.5:n.1566+151T>A
ENST00000482603.1:n.318+151T>A
ENST00000491488.5:n.570+151T>A
ENST00000494290.1:c.*51+1138T>A	ENSP00000432021.1:n.*51+1138T>A
ENST00000497693.1:n.4433+151T>A
ENST00000512404.2:n.203T>A
ENST00000607784.1:c.865+151T>A	ENSP00000475569.1:n.865+151T>A
NM_012203.1:c.865+151T>A	NP_036335.1:n.865+151T>A
XM_005251631.1:c.544+151T>A	XP_005251688.1:n.544+151T>A
XM_011518073.1:c.463+151T>A	XP_011516375.1:n.463+151T>A
XM_017015320.2:c.865+151T>A	XP_016870809.1:n.865+151T>A
XM_017015321.2:c.865+151T>A	XP_016870810.1:n.865+151T>A
XM_017015323.2:c.463+151T>A	XP_016870812.1:n.463+151T>A
XM_024447716.1:c.1138+151T>A	XP_024303484.1:n.1138+151T>A
XM_024447717.1:c.1138+151T>A	XP_024303485.1:n.1138+151T>A
XR_002956828.1:n.1153+151T>A
XR_002956829.1:n.1153+151T>A
XR_002956830.1:n.2285+151T>A
XR_002956831.1:n.1960+151T>A
XR_002956832.1:n.1284+151T>A
NM_012203.2:c.865+151T>A MANE Select	NP_036335.1:n.865+151T>A