Canonical Allele Identifier: CA2035831747
Gene: HIGD1C HGNC NCBI
SLC11A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.50963714A= , CM000674.2:g.50963714A= GRCh38
NC_000012.11:g.51357497A= , CM000674.1:g.51357497A= GRCh37
NC_000012.10:g.49643764A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000695929.1:c.*534+2612A= ENSP00000512272.1:n.*534+2612A=
ENST00000695930.1:c.253+2612A= (HIGD1C) ENSP00000512273.1:n.253+2612A=
ENST00000695931.1:c.229+2612A= (HIGD1C) MANE Select ENSP00000512274.1:n.229+2612A=
ENST00000398455.3:c.229+2612A= (HIGD1C) ENSP00000381473.3:n.229+2612A=
NM_001109619.1:c.229+2612A= (HIGD1C) NP_001103089.1:n.229+2612A=
XM_011538648.1:c.544+2612A= (HIGD1C) XP_011536950.1:n.544+2612A=
XM_011538649.1:c.229+2612A= (HIGD1C) XP_011536951.1:n.229+2612A=
NM_001109619.2:c.229+2612A= (HIGD1C) NP_001103089.1:n.229+2612A=
XM_011538649.2:c.229+2612A= (HIGD1C) XP_011536951.1:n.229+2612A=
XM_017019783.2:c.373+2612A= (HIGD1C) XP_016875272.1:n.373+2612A=
XM_017019784.2:c.373+2612A= (HIGD1C) XP_016875273.1:n.373+2612A=
XM_017019785.1:c.253+2612A= (HIGD1C) XP_016875274.1:n.253+2612A=
XR_001748720.1:n.1992-9906T= (SLC11A2)
NM_001109619.3:c.229+2612A= (HIGD1C) NP_001103089.1:n.229+2612A=
NM_001109619.4:c.229+2612A= (HIGD1C) MANE Select NP_001103089.1:n.229+2612A=