Canonical Allele Identifier: CA2333586077

Gene: HAMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35284906_35284907delinsGT , CM000681.2:g.35284906_35284907delinsGT	GRCh38
NC_000019.9:g.35775809_35775810delinsGT , CM000681.1:g.35775809_35775810delinsGT	GRCh37
NC_000019.8:g.40467649_40467650delinsGT	NCBI36
NG_011563.1:g.7400_7401delinsGT
NG_011563.2:g.7400_7401delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000222304.5:c.151-32_151-31delinsGT MANE Select	ENSP00000222304.2:n.151-32_151-31delinsGT...
ENST00000222304.3:c.151-32_151-31delinsGT	ENSP00000222304.2:n.151-32_151-31delinsGT...
ENST00000593580.1:n.2390_2391delinsGT
ENST00000598398.5:c.151-32_151-31delinsGT	ENSP00000471894.1:n.151-32_151-31delinsGT...
NM_021175.2:c.151-32_151-31delinsGT	NP_066998.1:n.151-32_151-31delinsGT
NM_021175.3:c.151-32_151-31delinsGT	NP_066998.1:n.151-32_151-31delinsGT
NM_021175.4:c.151-32_151-31delinsGT MANE Select	NP_066998.1:n.151-32_151-31delinsGT