Canonical Allele Identifier: CA1481306150

Gene: SLC39A8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102279363_102279366delinsCTAA , CM000666.2:g.102279363_102279366delinsCTAA	GRCh38
NC_000004.11:g.103200520_103200523delinsCTAA , CM000666.1:g.103200520_103200523delinsCTAA	GRCh37
NC_000004.10:g.103419543_103419546delinsCTAA	NCBI36
NG_047177.1:g.71133_71136delinsTTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424970.7:c.865+6583_865+6586delinsTTAG	ENSP00000394548.3:n.865+6583_865+6586delinsTTAG
ENST00000682227.1:c.841-11287_841-11284delinsTTAG	ENSP00000508363.1:n.841-11287_841-11284delinsTTAG
ENST00000682243.1:c.*986+6583_*986+6586delinsTTAG	ENSP00000507952.1:n.*986+6583_*986+6586delinsTTAG
ENST00000682549.1:c.865+6583_865+6586delinsTTAG	ENSP00000507483.1:n.865+6583_865+6586delinsTTAG
ENST00000682932.1:c.841-11287_841-11284delinsTTAG	ENSP00000507414.1:n.841-11287_841-11284delinsTTAG
ENST00000683173.1:c.*962-11287_*962-11284delinsTTAG	ENSP00000508032.1:n.*962-11287_*962-11284delinsTTAG
ENST00000683221.1:c.841-11287_841-11284delinsTTAG	ENSP00000508093.1:n.841-11287_841-11284delinsTTAG
ENST00000683401.1:n.774-11287_774-11284delinsTTAG
ENST00000683412.1:c.841-11287_841-11284delinsTTAG	ENSP00000507538.1:n.841-11287_841-11284delinsTTAG
ENST00000683462.1:c.865+6583_865+6586delinsTTAG	ENSP00000507170.1:n.865+6583_865+6586delinsTTAG
ENST00000683634.1:c.*962-11287_*962-11284delinsTTAG	ENSP00000507087.1:n.*962-11287_*962-11284delinsTTAG
ENST00000683706.1:c.244+6583_244+6586delinsTTAG	ENSP00000506745.1:n.244+6583_244+6586delinsTTAG
ENST00000683916.1:c.865+6583_865+6586delinsTTAG	ENSP00000508106.1:n.865+6583_865+6586delinsTTAG
ENST00000684289.1:c.*516-11287_*516-11284delinsTTAG	ENSP00000506748.1:n.*516-11287_*516-11284delinsTTAG
ENST00000684386.1:c.*54+2106_*54+2109delinsTTAG	ENSP00000507611.1:n.*54+2106_*54+2109delinsTTAG
ENST00000356736.5:c.841-11287_841-11284delinsTTAG MANE Select	ENSP00000349174.4:n.841-11287_841-11284delinsTTAG
ENST00000356736.4:c.841-11287_841-11284delinsTTAG	ENSP00000349174.4:n.841-11287_841-11284delinsTTAG
ENST00000394833.6:c.841-11287_841-11284delinsTTAG	ENSP00000378310.2:n.841-11287_841-11284delinsTTAG
ENST00000424970.6:c.841-11287_841-11284delinsTTAG	ENSP00000394548.2:n.841-11287_841-11284delinsTTAG
ENST00000512337.1:n.173-9572_173-9569delinsTTAG
NM_001135146.1:c.841-11287_841-11284delinsTTAG	NP_001128618.1:n.841-11287_841-11284delinsTTAG
NM_001135147.1:c.841-11287_841-11284delinsTTAG	NP_001128619.1:n.841-11287_841-11284delinsTTAG
NM_001135148.1:c.640-11287_640-11284delinsTTAG	NP_001128620.1:n.640-11287_640-11284delinsTTAG
NM_022154.5:c.841-11287_841-11284delinsTTAG	NP_071437.3:n.841-11287_841-11284delinsTTAG
XM_005263177.1:c.841-11287_841-11284delinsTTAG	XP_005263234.1:n.841-11287_841-11284delinsTTAG
XM_011532182.1:c.199-11287_199-11284delinsTTAG	XP_011530484.1:n.199-11287_199-11284delinsTTAG
XM_005263177.2:c.841-11287_841-11284delinsTTAG	XP_005263234.1:n.841-11287_841-11284delinsTTAG
XM_017008541.1:c.640-11287_640-11284delinsTTAG	XP_016864030.1:n.640-11287_640-11284delinsTTAG
XM_024454184.1:c.841-11287_841-11284delinsTTAG	XP_024309952.1:n.841-11287_841-11284delinsTTAG
NM_001135146.2:c.841-11287_841-11284delinsTTAG MANE Select	NP_001128618.1:n.841-11287_841-11284delinsTTAG
NM_001135148.2:c.640-11287_640-11284delinsTTAG	NP_001128620.1:n.640-11287_640-11284delinsTTAG