Canonical Allele Identifier: CA1481301276

Gene: SLC39A8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102268067_102268068delinsCT , CM000666.2:g.102268067_102268068delinsCT	GRCh38
NC_000004.11:g.103189224_103189225delinsCT , CM000666.1:g.103189224_103189225delinsCT	GRCh37
NC_000004.10:g.103408247_103408248delinsCT	NCBI36
NG_047177.1:g.82431_82432delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424970.7:c.877_878delinsAG	ENSP00000394548.3:p.Arg293=
ENST00000682227.1:c.852_853delinsAG	ENSP00000508363.1:p.Lys284=
ENST00000682243.1:c.*998_*999delinsAG	ENSP00000507952.1:n.*998_*999delinsAG
ENST00000682549.1:c.877_878delinsAG	ENSP00000507483.1:p.Arg293=
ENST00000682932.1:c.852_853delinsAG	ENSP00000507414.1:p.Lys284=
ENST00000683173.1:c.*973_*974delinsAG	ENSP00000508032.1:n.*973_*974delinsAG
ENST00000683221.1:c.852_853delinsAG	ENSP00000508093.1:p.Lys284=
ENST00000683401.1:n.785_786delinsAG
ENST00000683412.1:c.852_853delinsAG	ENSP00000507538.1:p.Lys284=
ENST00000683462.1:c.877_878delinsAG	ENSP00000507170.1:p.Arg293=
ENST00000683634.1:c.*973_*974delinsAG	ENSP00000507087.1:n.*973_*974delinsAG
ENST00000683706.1:c.256_257delinsAG	ENSP00000506745.1:p.Arg86=
ENST00000683916.1:c.877_878delinsAG	ENSP00000508106.1:p.Arg293=
ENST00000684289.1:c.*527_*528delinsAG	ENSP00000506748.1:n.*527_*528delinsAG
ENST00000684386.1:c.*66_*67delinsAG	ENSP00000507611.1:n.*66_*67delinsAG
ENST00000356736.5:c.852_853delinsAG MANE Select	ENSP00000349174.4:p.Lys284=
ENST00000356736.4:c.852_853delinsAG	ENSP00000349174.4:p.Lys284=
ENST00000394833.6:c.852_853delinsAG	ENSP00000378310.2:p.Lys284=
ENST00000424970.6:c.852_853delinsAG	ENSP00000394548.2:p.Lys284=
NM_001135146.1:c.852_853delinsAG	NP_001128618.1:p.Lys284=
NM_001135147.1:c.852_853delinsAG	NP_001128619.1:p.Lys284=
NM_001135148.1:c.651_652delinsAG	NP_001128620.1:p.Lys217=
NM_022154.5:c.852_853delinsAG	NP_071437.3:p.Lys284=
XM_005263177.1:c.852_853delinsAG	XP_005263234.1:p.Lys284=
XM_011532182.1:c.210_211delinsAG	XP_011530484.1:p.Lys70=
XM_005263177.2:c.852_853delinsAG	XP_005263234.1:p.Lys284=
XM_017008541.1:c.651_652delinsAG	XP_016864030.1:p.Lys217=
XM_024454184.1:c.852_853delinsAG	XP_024309952.1:p.Lys284=
NM_001135146.2:c.852_853delinsAG MANE Select	NP_001128618.1:p.Lys284=
NM_001135148.2:c.651_652delinsAG	NP_001128620.1:p.Lys217=