Canonical Allele Identifier: CA2035831787

Gene: HIGD1C SLC11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.50963802G= , CM000674.2:g.50963802G=	GRCh38
NC_000012.11:g.51357585G= , CM000674.1:g.51357585G=	GRCh37
NC_000012.10:g.49643852G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000695929.1:c.*534+2700G=	ENSP00000512272.1:n.*534+2700G=
ENST00000695930.1:c.253+2700G= (HIGD1C)	ENSP00000512273.1:n.253+2700G=
ENST00000695931.1:c.229+2700G= (HIGD1C) MANE Select	ENSP00000512274.1:n.229+2700G=
ENST00000398455.3:c.229+2700G= (HIGD1C)	ENSP00000381473.3:n.229+2700G=
NM_001109619.1:c.229+2700G= (HIGD1C)	NP_001103089.1:n.229+2700G=
XM_011538648.1:c.544+2700G= (HIGD1C)	XP_011536950.1:n.544+2700G=
XM_011538649.1:c.229+2700G= (HIGD1C)	XP_011536951.1:n.229+2700G=
NM_001109619.2:c.229+2700G= (HIGD1C)	NP_001103089.1:n.229+2700G=
XM_011538649.2:c.229+2700G= (HIGD1C)	XP_011536951.1:n.229+2700G=
XM_017019783.2:c.373+2700G= (HIGD1C)	XP_016875272.1:n.373+2700G=
XM_017019784.2:c.373+2700G= (HIGD1C)	XP_016875273.1:n.373+2700G=
XM_017019785.1:c.253+2700G= (HIGD1C)	XP_016875274.1:n.253+2700G=
XR_001748720.1:n.1992-9994C= (SLC11A2)
NM_001109619.3:c.229+2700G= (HIGD1C)	NP_001103089.1:n.229+2700G=
NM_001109619.4:c.229+2700G= (HIGD1C) MANE Select	NP_001103089.1:n.229+2700G=