Canonical Allele Identifier: CA1846868754

Gene: GRHPR

Linked Data

• dbSNP Id: rs1823182170
• gnomAD v4: 9-37428330-TGCAGTGCCGAGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428339_37428351del , CM000671.2:g.37428339_37428351del	GRCh38
NC_000009.11:g.37428336_37428348del , CM000671.1:g.37428336_37428348del	GRCh37
NC_000009.10:g.37418336_37418348del	NCBI36
NG_008135.1:g.10630_10642del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.405-145_405-133del MANE Select	ENSP00000313432.6:n.405-145_405-133del
ENST00000318158.10:c.405-145_405-133del	ENSP00000313432.6:n.405-145_405-133del
ENST00000377824.8:n.442-145_442-133del
ENST00000460882.5:n.432-145_432-133del
ENST00000491488.5:n.110-145_110-133del
ENST00000493368.5:n.462-145_462-133del
ENST00000497693.1:n.634_646del
ENST00000607784.1:c.405-145_405-133del	ENSP00000475569.1:n.405-145_405-133del
NM_012203.1:c.405-145_405-133del	NP_036335.1:n.405-145_405-133del
XM_005251631.1:c.84-145_84-133del	XP_005251688.1:n.84-145_84-133del
XM_011518073.1:c.-358-145_-358-133del	XP_011516375.1:n.-358-145_-358-133del
XR_929374.1:n.490-145_490-133del
XM_017015320.2:c.405-145_405-133del	XP_016870809.1:n.405-145_405-133del
XM_017015321.2:c.405-145_405-133del	XP_016870810.1:n.405-145_405-133del
XM_017015323.2:c.-358-145_-358-133del	XP_016870812.1:n.-358-145_-358-133del
XM_024447716.1:c.678-145_678-133del	XP_024303484.1:n.678-145_678-133del
XM_024447717.1:c.678-145_678-133del	XP_024303485.1:n.678-145_678-133del
XR_002956828.1:n.693-145_693-133del
XR_002956829.1:n.693-145_693-133del
XR_002956830.1:n.464-145_464-133del
XR_002956831.1:n.139-145_139-133del
XR_002956832.1:n.464-145_464-133del
NM_012203.2:c.405-145_405-133del MANE Select	NP_036335.1:n.405-145_405-133del