Canonical Allele Identifier: CA213878

Gene: GHRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30969977T>G , CM000669.2:g.30969977T>G	GRCh38
NC_000007.13:g.31009592T>G , CM000669.1:g.31009592T>G	GRCh37
NC_000007.12:g.30976117T>G	NCBI36
NG_021416.1:g.10957T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000823.4:c.366+13T>G MANE Select	NP_000814.2:n.366+13T>G
ENST00000326139.7:c.366+13T>G MANE Select	ENSP00000320180.2:n.366+13T>G
NM_000823.3:c.366+13T>G	NP_000814.2:n.366+13T>G
ENST00000326139.6:c.366+13T>G	ENSP00000320180.2:n.366+13T>G
ENST00000337750.9:c.174+13T>G	ENSP00000338184.4:n.174+13T>G
ENST00000396227.6:c.174+13T>G	ENSP00000379529.2:n.174+13T>G
ENST00000409316.5:c.-182+13T>G	ENSP00000386602.1:n.-182+13T>G
ENST00000409904.7:c.174+13T>G	ENSP00000387113.3:n.174+13T>G
XM_011515263.1:c.174+13T>G	XP_011513565.1:n.174+13T>G