Canonical Allele Identifier: CA2841200538

Gene: HAMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35285090C>T , CM000681.2:g.35285090C>T	GRCh38
NC_000019.9:g.35775993C>T , CM000681.1:g.35775993C>T	GRCh37
NC_000019.8:g.40467833C>T	NCBI36
NG_011563.1:g.7584C>T
NG_011563.2:g.7584C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222304.5:c.*48C>T MANE Select	ENSP00000222304.2:n.*48C>T
ENST00000222304.3:c.*48C>T	ENSP00000222304.2:n.*48C>T
ENST00000593580.1:n.2574C>T
ENST00000598398.5:c.*48C>T	ENSP00000471894.1:n.*48C>T
NM_021175.2:c.*48C>T	NP_066998.1:n.*48C>T
NM_021175.3:c.*48C>T	NP_066998.1:n.*48C>T
NM_021175.4:c.*48C>T MANE Select	NP_066998.1:n.*48C>T