Canonical Allele Identifier: CA2695195592
Gene: GHSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447387_172447389delinsGGA , CM000665.2:g.172447387_172447389delinsGGA GRCh38
NC_000003.11:g.172165177_172165179delinsGGA , CM000665.1:g.172165177_172165179delinsGGA GRCh37
NC_000003.10:g.173647871_173647873delinsGGA NCBI36
NG_021159.1:g.6068_6070delinsTCC

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+229_796+231delinsTCC MANE Select ENSP00000241256.2:n.796+229_796+231delins...
ENST00000241256.2:c.796+229_796+231delinsTCC ENSP00000241256.2:n.796+229_796+231delins...
NM_198407.2:c.796+229_796+231delinsTCC MANE Select NP_940799.1:n.796+229_796+231delinsTCC