Canonical Allele Identifier: CA2841002662

Gene: GHRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30968953dup , CM000669.2:g.30968953dup	GRCh38
NC_000007.13:g.31008568dup , CM000669.1:g.31008568dup	GRCh37
NC_000007.12:g.30975093dup	NCBI36
NG_021416.1:g.9933dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326139.7:c.160+17dup MANE Select	ENSP00000320180.2:n.160+17dup
ENST00000326139.6:c.160+17dup	ENSP00000320180.2:n.160+17dup
NM_000823.3:c.160+17dup	NP_000814.2:n.160+17dup
NM_000823.4:c.160+17dup MANE Select	NP_000814.2:n.160+17dup