Canonical Allele Identifier: CA1481306195

Gene: SLC39A8

Linked Data

• dbSNP Id: rs1732779305

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102279497C>G , CM000666.2:g.102279497C>G	GRCh38
NC_000004.11:g.103200654C>G , CM000666.1:g.103200654C>G	GRCh37
NC_000004.10:g.103419677C>G	NCBI36
NG_047177.1:g.71002G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000424970.7:c.865+6452G>C	ENSP00000394548.3:n.865+6452G>C
ENST00000682227.1:c.841-11418G>C	ENSP00000508363.1:n.841-11418G>C
ENST00000682243.1:c.*986+6452G>C	ENSP00000507952.1:n.*986+6452G>C
ENST00000682549.1:c.865+6452G>C	ENSP00000507483.1:n.865+6452G>C
ENST00000682932.1:c.841-11418G>C	ENSP00000507414.1:n.841-11418G>C
ENST00000683173.1:c.*962-11418G>C	ENSP00000508032.1:n.*962-11418G>C
ENST00000683221.1:c.841-11418G>C	ENSP00000508093.1:n.841-11418G>C
ENST00000683401.1:n.774-11418G>C
ENST00000683412.1:c.841-11418G>C	ENSP00000507538.1:n.841-11418G>C
ENST00000683462.1:c.865+6452G>C	ENSP00000507170.1:n.865+6452G>C
ENST00000683634.1:c.*962-11418G>C	ENSP00000507087.1:n.*962-11418G>C
ENST00000683706.1:c.244+6452G>C	ENSP00000506745.1:n.244+6452G>C
ENST00000683916.1:c.865+6452G>C	ENSP00000508106.1:n.865+6452G>C
ENST00000684289.1:c.*516-11418G>C	ENSP00000506748.1:n.*516-11418G>C
ENST00000684386.1:c.*54+1975G>C	ENSP00000507611.1:n.*54+1975G>C
ENST00000356736.5:c.841-11418G>C MANE Select	ENSP00000349174.4:n.841-11418G>C
ENST00000356736.4:c.841-11418G>C	ENSP00000349174.4:n.841-11418G>C
ENST00000394833.6:c.841-11418G>C	ENSP00000378310.2:n.841-11418G>C
ENST00000424970.6:c.841-11418G>C	ENSP00000394548.2:n.841-11418G>C
ENST00000512337.1:n.173-9703G>C
NM_001135146.1:c.841-11418G>C	NP_001128618.1:n.841-11418G>C
NM_001135147.1:c.841-11418G>C	NP_001128619.1:n.841-11418G>C
NM_001135148.1:c.640-11418G>C	NP_001128620.1:n.640-11418G>C
NM_022154.5:c.841-11418G>C	NP_071437.3:n.841-11418G>C
XM_005263177.1:c.841-11418G>C	XP_005263234.1:n.841-11418G>C
XM_011532182.1:c.199-11418G>C	XP_011530484.1:n.199-11418G>C
XM_005263177.2:c.841-11418G>C	XP_005263234.1:n.841-11418G>C
XM_017008541.1:c.640-11418G>C	XP_016864030.1:n.640-11418G>C
XM_024454184.1:c.841-11418G>C	XP_024309952.1:n.841-11418G>C
NM_001135146.2:c.841-11418G>C MANE Select	NP_001128618.1:n.841-11418G>C
NM_001135148.2:c.640-11418G>C	NP_001128620.1:n.640-11418G>C