Canonical Allele Identifier: CA2689954709

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37428588-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428591del , CM000671.2:g.37428591del	GRCh38
NC_000009.11:g.37428588del , CM000671.1:g.37428588del	GRCh37
NC_000009.10:g.37418588del	NCBI36
NG_008135.1:g.10882del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.493+19del MANE Select	ENSP00000313432.6:n.493+19del
ENST00000318158.10:c.493+19del	ENSP00000313432.6:n.493+19del
ENST00000377824.8:n.530+19del
ENST00000460882.5:n.520+19del
ENST00000480596.5:n.54del
ENST00000491488.5:n.198+19del
ENST00000493368.5:n.569del
ENST00000497693.1:n.886del
ENST00000607784.1:c.493+19del	ENSP00000475569.1:n.493+19del
NM_012203.1:c.493+19del	NP_036335.1:n.493+19del
XM_005251631.1:c.172+19del	XP_005251688.1:n.172+19del
XM_011518073.1:c.-251del	XP_011516375.1:n.-251del
XR_929374.1:n.597del
XM_017015320.2:c.493+19del	XP_016870809.1:n.493+19del
XM_017015321.2:c.493+19del	XP_016870810.1:n.493+19del
XM_017015323.2:c.-251del	XP_016870812.1:n.-251del
XM_024447716.1:c.766+19del	XP_024303484.1:n.766+19del
XM_024447717.1:c.766+19del	XP_024303485.1:n.766+19del
XR_002956828.1:n.781+19del
XR_002956829.1:n.781+19del
XR_002956830.1:n.552+19del
XR_002956831.1:n.227+19del
XR_002956832.1:n.571del
NM_012203.2:c.493+19del MANE Select	NP_036335.1:n.493+19del