Canonical Allele Identifier: CA102674236

Gene: SLC39A8

Linked Data

• dbSNP Id: rs555081607
• gnomAD v2: 4-103189290-TACAG-T
• gnomAD v3: 4-102268133-TACAG-T
• gnomAD v4: 4-102268133-TACAG-T
• MyVariant Identifiers: chr4:g.103189291_103189294del (hg19) ; chr4:g.102268134_102268137del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102268137_102268140del , CM000666.2:g.102268137_102268140del	GRCh38
NC_000004.11:g.103189294_103189297del , CM000666.1:g.103189294_103189297del	GRCh37
NC_000004.10:g.103408317_103408320del	NCBI36
NG_047177.1:g.82362_82365del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424970.7:c.866-58_866-55del	ENSP00000394548.3:n.866-58_866-55del
ENST00000682227.1:c.841-58_841-55del	ENSP00000508363.1:n.841-58_841-55del
ENST00000682243.1:c.*987-58_*987-55del	ENSP00000507952.1:n.*987-58_*987-55del
ENST00000682549.1:c.866-58_866-55del	ENSP00000507483.1:n.866-58_866-55del
ENST00000682932.1:c.841-58_841-55del	ENSP00000507414.1:n.841-58_841-55del
ENST00000683173.1:c.*962-58_*962-55del	ENSP00000508032.1:n.*962-58_*962-55del
ENST00000683221.1:c.841-58_841-55del	ENSP00000508093.1:n.841-58_841-55del
ENST00000683401.1:n.774-58_774-55del
ENST00000683412.1:c.841-58_841-55del	ENSP00000507538.1:n.841-58_841-55del
ENST00000683462.1:c.866-58_866-55del	ENSP00000507170.1:n.866-58_866-55del
ENST00000683634.1:c.*962-58_*962-55del	ENSP00000507087.1:n.*962-58_*962-55del
ENST00000683706.1:c.245-58_245-55del	ENSP00000506745.1:n.245-58_245-55del
ENST00000683916.1:c.866-58_866-55del	ENSP00000508106.1:n.866-58_866-55del
ENST00000684289.1:c.*516-58_*516-55del	ENSP00000506748.1:n.*516-58_*516-55del
ENST00000684386.1:c.*55-58_*55-55del	ENSP00000507611.1:n.*55-58_*55-55del
ENST00000356736.5:c.841-58_841-55del MANE Select	ENSP00000349174.4:n.841-58_841-55del
ENST00000356736.4:c.841-58_841-55del	ENSP00000349174.4:n.841-58_841-55del
ENST00000394833.6:c.841-58_841-55del	ENSP00000378310.2:n.841-58_841-55del
ENST00000424970.6:c.841-58_841-55del	ENSP00000394548.2:n.841-58_841-55del
NM_001135146.1:c.841-58_841-55del	NP_001128618.1:n.841-58_841-55del
NM_001135147.1:c.841-58_841-55del	NP_001128619.1:n.841-58_841-55del
NM_001135148.1:c.640-58_640-55del	NP_001128620.1:n.640-58_640-55del
NM_022154.5:c.841-58_841-55del	NP_071437.3:n.841-58_841-55del
XM_005263177.1:c.841-58_841-55del	XP_005263234.1:n.841-58_841-55del
XM_011532182.1:c.199-58_199-55del	XP_011530484.1:n.199-58_199-55del
XM_005263177.2:c.841-58_841-55del	XP_005263234.1:n.841-58_841-55del
XM_017008541.1:c.640-58_640-55del	XP_016864030.1:n.640-58_640-55del
XM_024454184.1:c.841-58_841-55del	XP_024309952.1:n.841-58_841-55del
NM_001135146.2:c.841-58_841-55del MANE Select	NP_001128618.1:n.841-58_841-55del
NM_001135148.2:c.640-58_640-55del	NP_001128620.1:n.640-58_640-55del