Canonical Allele Identifier: CA1697966094

Gene: GHRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30979349A= , CM000669.2:g.30979349A=	GRCh38
NC_000007.13:g.31018964A= , CM000669.1:g.31018964A=	GRCh37
NC_000007.12:g.30985489A=	NCBI36
NG_021416.1:g.20329A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326139.7:c.*105A= MANE Select	ENSP00000320180.2:n.*105A=
ENST00000326139.6:c.*105A=	ENSP00000320180.2:n.*105A=
ENST00000337750.9:c.*593A=	ENSP00000338184.4:n.*593A=
ENST00000396227.6:c.*593A=	ENSP00000379529.2:n.*593A=
ENST00000409316.5:c.*220A=	ENSP00000386602.1:n.*220A=
ENST00000409904.7:c.*105A=	ENSP00000387113.3:n.*105A=
ENST00000461424.5:n.680+2791A=
ENST00000463164.1:n.361A=
ENST00000611037.1:c.550+2791A=	ENSP00000480159.1:n.550+2791A=
NM_000823.3:c.*105A=	NP_000814.2:n.*105A=
XM_011515263.1:c.*105A=	XP_011513565.1:n.*105A=
NM_000823.4:c.*105A= MANE Select	NP_000814.2:n.*105A=