Canonical Allele Identifier: CA1697966138
Gene: GHRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30979363A= , CM000669.2:g.30979363A= GRCh38
NC_000007.13:g.31018978A= , CM000669.1:g.31018978A= GRCh37
NC_000007.12:g.30985503A= NCBI36
NG_021416.1:g.20343A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326139.7:c.*119A= MANE Select ENSP00000320180.2:n.*119A=
ENST00000326139.6:c.*119A= ENSP00000320180.2:n.*119A=
ENST00000337750.9:c.*607A= ENSP00000338184.4:n.*607A=
ENST00000396227.6:c.*607A= ENSP00000379529.2:n.*607A=
ENST00000409316.5:c.*234A= ENSP00000386602.1:n.*234A=
ENST00000409904.7:c.*119A= ENSP00000387113.3:n.*119A=
ENST00000461424.5:n.680+2805A=
ENST00000463164.1:n.375A=
ENST00000611037.1:c.550+2805A= ENSP00000480159.1:n.550+2805A=
NM_000823.3:c.*119A= NP_000814.2:n.*119A=
XM_011515263.1:c.*119A= XP_011513565.1:n.*119A=
NM_000823.4:c.*119A= MANE Select NP_000814.2:n.*119A=