Canonical Allele Identifier: CA2689953944

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37428102-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428104_37428105del , CM000671.2:g.37428104_37428105del	GRCh38
NC_000009.11:g.37428101_37428102del , CM000671.1:g.37428101_37428102del	GRCh37
NC_000009.10:g.37418101_37418102del	NCBI36
NG_008135.1:g.10395_10396del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.405-380_405-379del MANE Select	ENSP00000313432.6:n.405-380_405-379del
ENST00000318158.10:c.405-380_405-379del	ENSP00000313432.6:n.405-380_405-379del
ENST00000377824.8:n.442-380_442-379del
ENST00000460882.5:n.432-380_432-379del
ENST00000491488.5:n.110-380_110-379del
ENST00000493368.5:n.462-380_462-379del
ENST00000497693.1:n.399_400del
ENST00000607784.1:c.405-380_405-379del	ENSP00000475569.1:n.405-380_405-379del
NM_012203.1:c.405-380_405-379del	NP_036335.1:n.405-380_405-379del
XM_005251631.1:c.84-380_84-379del	XP_005251688.1:n.84-380_84-379del
XM_011518073.1:c.-358-380_-358-379del	XP_011516375.1:n.-358-380_-358-379del
XR_929374.1:n.490-380_490-379del
XM_017015320.2:c.405-380_405-379del	XP_016870809.1:n.405-380_405-379del
XM_017015321.2:c.405-380_405-379del	XP_016870810.1:n.405-380_405-379del
XM_017015323.2:c.-358-380_-358-379del	XP_016870812.1:n.-358-380_-358-379del
XM_024447716.1:c.678-380_678-379del	XP_024303484.1:n.678-380_678-379del
XM_024447717.1:c.678-380_678-379del	XP_024303485.1:n.678-380_678-379del
XR_002956828.1:n.693-380_693-379del
XR_002956829.1:n.693-380_693-379del
XR_002956830.1:n.464-380_464-379del
XR_002956831.1:n.139-380_139-379del
XR_002956832.1:n.464-380_464-379del
NM_012203.2:c.405-380_405-379del MANE Select	NP_036335.1:n.405-380_405-379del