Canonical Allele Identifier: CA2689984723

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436974-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436977del , CM000671.2:g.37436977del	GRCh38
NC_000009.11:g.37436974del , CM000671.1:g.37436974del	GRCh37
NC_000009.10:g.37426974del	NCBI36
NG_008135.1:g.19268del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*195del MANE Select	ENSP00000313432.6:n.*195del
ENST00000318158.10:c.*195del	ENSP00000313432.6:n.*195del
ENST00000480596.5:n.1883del
ENST00000494290.1:c.*148del	ENSP00000432021.1:n.*148del
ENST00000497693.1:n.4750del
NM_012203.1:c.*195del	NP_036335.1:n.*195del
XM_005251631.1:c.*195del	XP_005251688.1:n.*195del
XM_011518073.1:c.*195del	XP_011516375.1:n.*195del
XM_017015320.2:c.946-434del	XP_016870809.1:n.946-434del
XM_017015321.2:c.866-434del	XP_016870810.1:n.866-434del
XM_017015323.2:c.544-434del	XP_016870812.1:n.544-434del
XM_024447716.1:c.1219-434del	XP_024303484.1:n.1219-434del
XM_024447717.1:c.1139-434del	XP_024303485.1:n.1139-434del
XR_002956828.1:n.1234-434del
XR_002956829.1:n.1154-434del
XR_002956830.1:n.2602del
XR_002956831.1:n.2277del
XR_002956832.1:n.1601del
NM_012203.2:c.*195del MANE Select	NP_036335.1:n.*195del