Canonical Allele Identifier: CA1697966255

Gene: GHRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30979442C= , CM000669.2:g.30979442C=	GRCh38
NC_000007.13:g.31019057C= , CM000669.1:g.31019057C=	GRCh37
NC_000007.12:g.30985582C=	NCBI36
NG_021416.1:g.20422C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326139.7:c.*198C= MANE Select	ENSP00000320180.2:n.*198C=
ENST00000326139.6:c.*198C=	ENSP00000320180.2:n.*198C=
ENST00000337750.9:c.*686C=	ENSP00000338184.4:n.*686C=
ENST00000396227.6:c.*686C=	ENSP00000379529.2:n.*686C=
ENST00000409316.5:c.*313C=	ENSP00000386602.1:n.*313C=
ENST00000409904.7:c.*198C=	ENSP00000387113.3:n.*198C=
ENST00000461424.5:n.680+2884C=
ENST00000463164.1:n.454C=
ENST00000611037.1:c.550+2884C=	ENSP00000480159.1:n.550+2884C=
NM_000823.3:c.*198C=	NP_000814.2:n.*198C=
XM_011515263.1:c.*198C=	XP_011513565.1:n.*198C=
NM_000823.4:c.*198C= MANE Select	NP_000814.2:n.*198C=