Canonical Allele Identifier: CA1697966260

Gene: GHRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30979446T= , CM000669.2:g.30979446T=	GRCh38
NC_000007.13:g.31019061T= , CM000669.1:g.31019061T=	GRCh37
NC_000007.12:g.30985586T=	NCBI36
NG_021416.1:g.20426T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326139.7:c.*202T= MANE Select	ENSP00000320180.2:n.*202T=
ENST00000326139.6:c.*202T=	ENSP00000320180.2:n.*202T=
ENST00000337750.9:c.*690T=	ENSP00000338184.4:n.*690T=
ENST00000396227.6:c.*690T=	ENSP00000379529.2:n.*690T=
ENST00000409316.5:c.*317T=	ENSP00000386602.1:n.*317T=
ENST00000409904.7:c.*202T=	ENSP00000387113.3:n.*202T=
ENST00000461424.5:n.680+2888T=
ENST00000463164.1:n.458T=
ENST00000611037.1:c.550+2888T=	ENSP00000480159.1:n.550+2888T=
NM_000823.3:c.*202T=	NP_000814.2:n.*202T=
XM_011515263.1:c.*202T=	XP_011513565.1:n.*202T=
NM_000823.4:c.*202T= MANE Select	NP_000814.2:n.*202T=