Canonical Allele Identifier: CA192889800

Gene: GRHPR

Linked Data

• dbSNP Id: rs376781208
• gnomAD v3: 9-37428806-CA-C
• gnomAD v4: 9-37428806-CA-C
• MyVariant Identifiers: chr9:g.37428804del (hg19) ; chr9:g.37428807del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428807del , CM000671.2:g.37428807del	GRCh38
NC_000009.11:g.37428804del , CM000671.1:g.37428804del	GRCh37
NC_000009.10:g.37418804del	NCBI36
NG_008135.1:g.11098del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.493+235del MANE Select	ENSP00000313432.6:n.493+235del
ENST00000318158.10:c.493+235del	ENSP00000313432.6:n.493+235del
ENST00000377824.8:n.530+235del
ENST00000460882.5:n.520+235del
ENST00000480596.5:n.270del
ENST00000491488.5:n.198+235del
ENST00000493368.5:n.785del
ENST00000497693.1:n.1102del
ENST00000607784.1:c.493+235del	ENSP00000475569.1:n.493+235del
NM_012203.1:c.493+235del	NP_036335.1:n.493+235del
XM_005251631.1:c.172+235del	XP_005251688.1:n.172+235del
XM_011518073.1:c.-35del	XP_011516375.1:n.-35del
XR_929374.1:n.813del
XM_017015320.2:c.493+235del	XP_016870809.1:n.493+235del
XM_017015321.2:c.493+235del	XP_016870810.1:n.493+235del
XM_017015323.2:c.-35del	XP_016870812.1:n.-35del
XM_024447716.1:c.766+235del	XP_024303484.1:n.766+235del
XM_024447717.1:c.766+235del	XP_024303485.1:n.766+235del
XR_002956828.1:n.781+235del
XR_002956829.1:n.781+235del
XR_002956830.1:n.552+235del
XR_002956831.1:n.227+235del
XR_002956832.1:n.787del
NM_012203.2:c.493+235del MANE Select	NP_036335.1:n.493+235del