Canonical Allele Identifier: CA2689954214

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37428353-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428354_37428355insAA , CM000671.2:g.37428354_37428355insAA	GRCh38
NC_000009.11:g.37428351_37428352insAA , CM000671.1:g.37428351_37428352insAA	GRCh37
NC_000009.10:g.37418351_37418352insAA	NCBI36
NG_008135.1:g.10645_10646insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.405-130_405-129insAA MANE Select	ENSP00000313432.6:n.405-130_405-129insAA
ENST00000318158.10:c.405-130_405-129insAA	ENSP00000313432.6:n.405-130_405-129insAA
ENST00000377824.8:n.442-130_442-129insAA
ENST00000460882.5:n.432-130_432-129insAA
ENST00000491488.5:n.110-130_110-129insAA
ENST00000493368.5:n.462-130_462-129insAA
ENST00000497693.1:n.649_650insAA
ENST00000607784.1:c.405-130_405-129insAA	ENSP00000475569.1:n.405-130_405-129insAA
NM_012203.1:c.405-130_405-129insAA	NP_036335.1:n.405-130_405-129insAA
XM_005251631.1:c.84-130_84-129insAA	XP_005251688.1:n.84-130_84-129insAA
XM_011518073.1:c.-358-130_-358-129insAA	XP_011516375.1:n.-358-130_-358-129insAA
XR_929374.1:n.490-130_490-129insAA
XM_017015320.2:c.405-130_405-129insAA	XP_016870809.1:n.405-130_405-129insAA
XM_017015321.2:c.405-130_405-129insAA	XP_016870810.1:n.405-130_405-129insAA
XM_017015323.2:c.-358-130_-358-129insAA	XP_016870812.1:n.-358-130_-358-129insAA
XM_024447716.1:c.678-130_678-129insAA	XP_024303484.1:n.678-130_678-129insAA
XM_024447717.1:c.678-130_678-129insAA	XP_024303485.1:n.678-130_678-129insAA
XR_002956828.1:n.693-130_693-129insAA
XR_002956829.1:n.693-130_693-129insAA
XR_002956830.1:n.464-130_464-129insAA
XR_002956831.1:n.139-130_139-129insAA
XR_002956832.1:n.464-130_464-129insAA
NM_012203.2:c.405-130_405-129insAA MANE Select	NP_036335.1:n.405-130_405-129insAA