Canonical Allele Identifier: CA2333586091

Gene: HAMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35284924_35284925delinsCT , CM000681.2:g.35284924_35284925delinsCT	GRCh38
NC_000019.9:g.35775827_35775828delinsCT , CM000681.1:g.35775827_35775828delinsCT	GRCh37
NC_000019.8:g.40467667_40467668delinsCT	NCBI36
NG_011563.1:g.7418_7419delinsCT
NG_011563.2:g.7418_7419delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000222304.5:c.151-14_151-13delinsCT MANE Select	ENSP00000222304.2:n.151-14_151-13delinsCT...
ENST00000222304.3:c.151-14_151-13delinsCT	ENSP00000222304.2:n.151-14_151-13delinsCT...
ENST00000593580.1:n.2408_2409delinsCT
ENST00000598398.5:c.151-14_151-13delinsCT	ENSP00000471894.1:n.151-14_151-13delinsCT...
NM_021175.2:c.151-14_151-13delinsCT	NP_066998.1:n.151-14_151-13delinsCT
NM_021175.3:c.151-14_151-13delinsCT	NP_066998.1:n.151-14_151-13delinsCT
NM_021175.4:c.151-14_151-13delinsCT MANE Select	NP_066998.1:n.151-14_151-13delinsCT