Canonical Allele Identifier: CA2689953263

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37426627-TGCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37426629_37426631del , CM000671.2:g.37426629_37426631del	GRCh38
NC_000009.11:g.37426626_37426628del , CM000671.1:g.37426626_37426628del	GRCh37
NC_000009.10:g.37416626_37416628del	NCBI36
NG_008135.1:g.8920_8922del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.379_381del MANE Select	ENSP00000313432.6:p.Pro127del
ENST00000318158.10:c.379_381del	ENSP00000313432.6:p.Pro127del
ENST00000377824.8:n.416_418del
ENST00000460882.5:n.406_408del
ENST00000487399.5:n.931_933del
ENST00000491488.5:n.110-1855_110-1853del
ENST00000493368.5:n.436_438del
ENST00000607784.1:c.379_381del	ENSP00000475569.1:p.Pro127del
NM_012203.1:c.379_381del	NP_036335.1:p.Pro127del
XM_005251631.1:c.84-1855_84-1853del	XP_005251688.1:n.84-1855_84-1853del
XM_011518073.1:c.-384_-382del	XP_011516375.1:n.-384_-382del
XR_929374.1:n.464_466del
XM_017015320.2:c.379_381del	XP_016870809.1:p.Pro127del
XM_017015321.2:c.379_381del	XP_016870810.1:p.Pro127del
XM_017015323.2:c.-384_-382del	XP_016870812.1:n.-384_-382del
XM_024447716.1:c.652_654del	XP_024303484.1:p.Pro218del
XM_024447717.1:c.652_654del	XP_024303485.1:p.Pro218del
XR_002956828.1:n.667_669del
XR_002956829.1:n.667_669del
XR_002956830.1:n.438_440del
XR_002956831.1:n.139-1855_139-1853del
XR_002956832.1:n.438_440del
NM_012203.2:c.379_381del MANE Select	NP_036335.1:p.Pro127del