Canonical Allele Identifier: CA2584453449

Gene: HAMP

Linked Data

• gnomAD v4: 19-35284863-GATGCCTTTCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35284864_35284873del , CM000681.2:g.35284864_35284873del	GRCh38
NC_000019.9:g.35775767_35775776del , CM000681.1:g.35775767_35775776del	GRCh37
NC_000019.8:g.40467607_40467616del	NCBI36
NG_011563.1:g.7358_7367del
NG_011563.2:g.7358_7367del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222304.5:c.150+16_150+25del MANE Select	ENSP00000222304.2:n.150+16_150+25del
ENST00000222304.3:c.150+16_150+25del	ENSP00000222304.2:n.150+16_150+25del
ENST00000593580.1:n.2348_2357del
ENST00000598398.5:c.150+16_150+25del	ENSP00000471894.1:n.150+16_150+25del
NM_021175.2:c.150+16_150+25del	NP_066998.1:n.150+16_150+25del
NM_021175.3:c.150+16_150+25del	NP_066998.1:n.150+16_150+25del
NM_021175.4:c.150+16_150+25del MANE Select	NP_066998.1:n.150+16_150+25del