Canonical Allele Identifier: CA102677471

Gene: SLC39A8

Linked Data

• dbSNP Id: rs925616781
• MyVariant Identifiers: chr4:g.103200455_103200458del (hg19) ; chr4:g.102279298_102279301del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102279304_102279307del , CM000666.2:g.102279304_102279307del	GRCh38
NC_000004.11:g.103200461_103200464del , CM000666.1:g.103200461_103200464del	GRCh37
NC_000004.10:g.103419484_103419487del	NCBI36
NG_047177.1:g.71198_71201del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424970.7:c.865+6648_865+6651del	ENSP00000394548.3:n.865+6648_865+6651del
ENST00000682227.1:c.841-11222_841-11219del	ENSP00000508363.1:n.841-11222_841-11219del
ENST00000682243.1:c.*986+6648_*986+6651del	ENSP00000507952.1:n.*986+6648_*986+6651del
ENST00000682549.1:c.865+6648_865+6651del	ENSP00000507483.1:n.865+6648_865+6651del
ENST00000682932.1:c.841-11222_841-11219del	ENSP00000507414.1:n.841-11222_841-11219del
ENST00000683173.1:c.*962-11222_*962-11219del	ENSP00000508032.1:n.*962-11222_*962-11219del
ENST00000683221.1:c.841-11222_841-11219del	ENSP00000508093.1:n.841-11222_841-11219del
ENST00000683401.1:n.774-11222_774-11219del
ENST00000683412.1:c.841-11222_841-11219del	ENSP00000507538.1:n.841-11222_841-11219del
ENST00000683462.1:c.865+6648_865+6651del	ENSP00000507170.1:n.865+6648_865+6651del
ENST00000683634.1:c.*962-11222_*962-11219del	ENSP00000507087.1:n.*962-11222_*962-11219del
ENST00000683706.1:c.244+6648_244+6651del	ENSP00000506745.1:n.244+6648_244+6651del
ENST00000683916.1:c.865+6648_865+6651del	ENSP00000508106.1:n.865+6648_865+6651del
ENST00000684289.1:c.*516-11222_*516-11219del	ENSP00000506748.1:n.*516-11222_*516-11219del
ENST00000684386.1:c.*54+2171_*54+2174del	ENSP00000507611.1:n.*54+2171_*54+2174del
ENST00000356736.5:c.841-11222_841-11219del MANE Select	ENSP00000349174.4:n.841-11222_841-11219del
ENST00000356736.4:c.841-11222_841-11219del	ENSP00000349174.4:n.841-11222_841-11219del
ENST00000394833.6:c.841-11222_841-11219del	ENSP00000378310.2:n.841-11222_841-11219del
ENST00000424970.6:c.841-11222_841-11219del	ENSP00000394548.2:n.841-11222_841-11219del
ENST00000512337.1:n.173-9507_173-9504del
NM_001135146.1:c.841-11222_841-11219del	NP_001128618.1:n.841-11222_841-11219del
NM_001135147.1:c.841-11222_841-11219del	NP_001128619.1:n.841-11222_841-11219del
NM_001135148.1:c.640-11222_640-11219del	NP_001128620.1:n.640-11222_640-11219del
NM_022154.5:c.841-11222_841-11219del	NP_071437.3:n.841-11222_841-11219del
XM_005263177.1:c.841-11222_841-11219del	XP_005263234.1:n.841-11222_841-11219del
XM_011532182.1:c.199-11222_199-11219del	XP_011530484.1:n.199-11222_199-11219del
XM_005263177.2:c.841-11222_841-11219del	XP_005263234.1:n.841-11222_841-11219del
XM_017008541.1:c.640-11222_640-11219del	XP_016864030.1:n.640-11222_640-11219del
XM_024454184.1:c.841-11222_841-11219del	XP_024309952.1:n.841-11222_841-11219del
NM_001135146.2:c.841-11222_841-11219del MANE Select	NP_001128618.1:n.841-11222_841-11219del
NM_001135148.2:c.640-11222_640-11219del	NP_001128620.1:n.640-11222_640-11219del