Canonical Allele Identifier: CA2682271979

Gene: GHRHR

Linked Data

• gnomAD v4: 7-30979346-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30979348del , CM000669.2:g.30979348del	GRCh38
NC_000007.13:g.31018963del , CM000669.1:g.31018963del	GRCh37
NC_000007.12:g.30985488del	NCBI36
NG_021416.1:g.20328del

Transcript Alleles

HGVS	Amino-acid change
ENST00000326139.7:c.*104del MANE Select	ENSP00000320180.2:n.*104del
ENST00000326139.6:c.*104del	ENSP00000320180.2:n.*104del
ENST00000337750.9:c.*592del	ENSP00000338184.4:n.*592del
ENST00000396227.6:c.*592del	ENSP00000379529.2:n.*592del
ENST00000409316.5:c.*219del	ENSP00000386602.1:n.*219del
ENST00000409904.7:c.*104del	ENSP00000387113.3:n.*104del
ENST00000461424.5:n.680+2790del
ENST00000463164.1:n.360del
ENST00000611037.1:c.550+2790del	ENSP00000480159.1:n.550+2790del
NM_000823.3:c.*104del	NP_000814.2:n.*104del
XM_011515263.1:c.*104del	XP_011513565.1:n.*104del
NM_000823.4:c.*104del MANE Select	NP_000814.2:n.*104del