Canonical Allele Identifier: CA2584453469

Gene: HAMP

Linked Data

• gnomAD v4: 19-35284889-T-TATCATTAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35284889_35284890insATCATTAAAAAA , CM000681.2:g.35284889_35284890insATCATTAAAAAA	GRCh38
NC_000019.9:g.35775792_35775793insATCATTAAAAAA , CM000681.1:g.35775792_35775793insATCATTAAAAAA	GRCh37
NC_000019.8:g.40467632_40467633insATCATTAAAAAA	NCBI36
NG_011563.1:g.7383_7384insATCATTAAAAAA
NG_011563.2:g.7383_7384insATCATTAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222304.5:c.150+41_150+42insATCATTAAAAAA MANE Select	ENSP00000222304.2:n.150+41_150+42insATCATTAAAAAA
ENST00000222304.3:c.150+41_150+42insATCATTAAAAAA	ENSP00000222304.2:n.150+41_150+42insATCATTAAAAAA
ENST00000593580.1:n.2373_2374insATCATTAAAAAA
ENST00000598398.5:c.150+41_150+42insATCATTAAAAAA	ENSP00000471894.1:n.150+41_150+42insATCATTAAAAAA
NM_021175.2:c.150+41_150+42insATCATTAAAAAA	NP_066998.1:n.150+41_150+42insATCATTAAAAAA
NM_021175.3:c.150+41_150+42insATCATTAAAAAA	NP_066998.1:n.150+41_150+42insATCATTAAAAAA
NM_021175.4:c.150+41_150+42insATCATTAAAAAA MANE Select	NP_066998.1:n.150+41_150+42insATCATTAAAAAA