Canonical Allele Identifier: CA784519555

Gene: SLC39A8

Linked Data

• dbSNP Id: rs1335907727
• gnomAD v3: 4-102268144-T-TG
• gnomAD v4: 4-102268144-T-TG
• MyVariant Identifiers: chr4:g.103189301_103189302insG (hg19) ; chr4:g.102268144_102268145insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102268146dup , CM000666.2:g.102268146dup	GRCh38
NC_000004.11:g.103189303dup , CM000666.1:g.103189303dup	GRCh37
NC_000004.10:g.103408326dup	NCBI36
NG_047177.1:g.82354dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424970.7:c.866-66dup	ENSP00000394548.3:n.866-66dup
ENST00000682227.1:c.841-66dup	ENSP00000508363.1:n.841-66dup
ENST00000682243.1:c.*987-66dup	ENSP00000507952.1:n.*987-66dup
ENST00000682549.1:c.866-66dup	ENSP00000507483.1:n.866-66dup
ENST00000682932.1:c.841-66dup	ENSP00000507414.1:n.841-66dup
ENST00000683173.1:c.*962-66dup	ENSP00000508032.1:n.*962-66dup
ENST00000683221.1:c.841-66dup	ENSP00000508093.1:n.841-66dup
ENST00000683401.1:n.774-66dup
ENST00000683412.1:c.841-66dup	ENSP00000507538.1:n.841-66dup
ENST00000683462.1:c.866-66dup	ENSP00000507170.1:n.866-66dup
ENST00000683634.1:c.*962-66dup	ENSP00000507087.1:n.*962-66dup
ENST00000683706.1:c.245-66dup	ENSP00000506745.1:n.245-66dup
ENST00000683916.1:c.866-66dup	ENSP00000508106.1:n.866-66dup
ENST00000684289.1:c.*516-66dup	ENSP00000506748.1:n.*516-66dup
ENST00000684386.1:c.*55-66dup	ENSP00000507611.1:n.*55-66dup
ENST00000356736.5:c.841-66dup MANE Select	ENSP00000349174.4:n.841-66dup
ENST00000356736.4:c.841-66dup	ENSP00000349174.4:n.841-66dup
ENST00000394833.6:c.841-66dup	ENSP00000378310.2:n.841-66dup
ENST00000424970.6:c.841-66dup	ENSP00000394548.2:n.841-66dup
NM_001135146.1:c.841-66dup	NP_001128618.1:n.841-66dup
NM_001135147.1:c.841-66dup	NP_001128619.1:n.841-66dup
NM_001135148.1:c.640-66dup	NP_001128620.1:n.640-66dup
NM_022154.5:c.841-66dup	NP_071437.3:n.841-66dup
XM_005263177.1:c.841-66dup	XP_005263234.1:n.841-66dup
XM_011532182.1:c.199-66dup	XP_011530484.1:n.199-66dup
XM_005263177.2:c.841-66dup	XP_005263234.1:n.841-66dup
XM_017008541.1:c.640-66dup	XP_016864030.1:n.640-66dup
XM_024454184.1:c.841-66dup	XP_024309952.1:n.841-66dup
NM_001135146.2:c.841-66dup MANE Select	NP_001128618.1:n.841-66dup
NM_001135148.2:c.640-66dup	NP_001128620.1:n.640-66dup