Canonical Allele Identifier: CA913157689

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37428528_37428537del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428531_37428540del , CM000671.2:g.37428531_37428540del	GRCh38
NC_000009.11:g.37428528_37428537del , CM000671.1:g.37428528_37428537del	GRCh37
NC_000009.10:g.37418528_37418537del	NCBI36
NG_008135.1:g.10822_10831del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.452_461del MANE Select	ENSP00000313432.6:p.Leu151ProfsTer11
ENST00000318158.10:c.452_461del	ENSP00000313432.6:p.Leu151ProfsTer11
ENST00000377824.8:n.489_498del
ENST00000460882.5:n.479_488del
ENST00000491488.5:n.157_166del
ENST00000493368.5:n.509_518del
ENST00000497693.1:n.826_835del
ENST00000607784.1:c.452_461del	ENSP00000475569.1:p.Leu151ProfsTer11
NM_012203.1:c.452_461del	NP_036335.1:p.Leu151ProfsTer11
XM_005251631.1:c.131_140del	XP_005251688.1:p.Leu44ProfsTer11
XM_011518073.1:c.-311_-302del	XP_011516375.1:n.-311_-302del
XR_929374.1:n.537_546del
XM_017015320.2:c.452_461del	XP_016870809.1:p.Leu151ProfsTer11
XM_017015321.2:c.452_461del	XP_016870810.1:p.Leu151ProfsTer11
XM_017015323.2:c.-311_-302del	XP_016870812.1:n.-311_-302del
XM_024447716.1:c.725_734del	XP_024303484.1:p.Leu242ProfsTer11
XM_024447717.1:c.725_734del	XP_024303485.1:p.Leu242ProfsTer11
XR_002956828.1:n.740_749del
XR_002956829.1:n.740_749del
XR_002956830.1:n.511_520del
XR_002956831.1:n.186_195del
XR_002956832.1:n.511_520del
NM_012203.2:c.452_461del MANE Select	NP_036335.1:p.Leu151ProfsTer11