Canonical Allele Identifier: CA367150354

Gene: GHRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30969961G>C , CM000669.2:g.30969961G>C	GRCh38
NC_000007.13:g.31009576G>C , CM000669.1:g.31009576G>C	GRCh37
NC_000007.12:g.30976101G>C	NCBI36
NG_021416.1:g.10941G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326139.7:c.363G>C MANE Select	ENSP00000320180.2:p.Glu121Asp
ENST00000326139.6:c.363G>C	ENSP00000320180.2:p.Glu121Asp
ENST00000337750.9:c.171G>C	ENSP00000338184.4:p.Glu57Asp
ENST00000396227.6:c.171G>C	ENSP00000379529.2:p.Glu57Asp
ENST00000409316.5:c.-185G>C	ENSP00000386602.1:n.-185G>C
ENST00000409904.7:c.171G>C	ENSP00000387113.3:p.Glu57Asp
NM_000823.3:c.363G>C	NP_000814.2:p.Glu121Asp
XM_011515263.1:c.171G>C	XP_011513565.1:p.Glu57Asp
NM_000823.4:c.363G>C MANE Select	NP_000814.2:p.Glu121Asp