Canonical Allele Identifier: CA1697966289

Gene: GHRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30979469C= , CM000669.2:g.30979469C=	GRCh38
NC_000007.13:g.31019084C= , CM000669.1:g.31019084C=	GRCh37
NC_000007.12:g.30985609C=	NCBI36
NG_021416.1:g.20449C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326139.7:c.*225C= MANE Select	ENSP00000320180.2:n.*225C=
ENST00000326139.6:c.*225C=	ENSP00000320180.2:n.*225C=
ENST00000337750.9:c.*713C=	ENSP00000338184.4:n.*713C=
ENST00000396227.6:c.*713C=	ENSP00000379529.2:n.*713C=
ENST00000409316.5:c.*340C=	ENSP00000386602.1:n.*340C=
ENST00000409904.7:c.*225C=	ENSP00000387113.3:n.*225C=
ENST00000461424.5:n.680+2911C=
ENST00000463164.1:n.481C=
ENST00000611037.1:c.550+2911C=	ENSP00000480159.1:n.550+2911C=
NM_000823.3:c.*225C=	NP_000814.2:n.*225C=
XM_011515263.1:c.*225C=	XP_011513565.1:n.*225C=
NM_000823.4:c.*225C= MANE Select	NP_000814.2:n.*225C=