Canonical Allele Identifier: CA1826306879

Gene: SLC39A4

Linked Data

• dbSNP Id: rs1822037798

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414007_144414009del , CM000670.2:g.144414007_144414009del	GRCh38
NC_000008.10:g.145639391_145639393del , CM000670.1:g.145639391_145639393del	GRCh37
NC_000008.9:g.145610199_145610201del	NCBI36
NG_012234.2:g.7886_7888del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1240_1242del MANE Select	ENSP00000301305.4:p.Phe414del
ENST00000276833.9:c.1165_1167del	ENSP00000276833.5:p.Phe389del
ENST00000301305.7:c.1240_1242del	ENSP00000301305.3:p.Phe414del
ENST00000531789.1:n.77_79del
NM_017767.2:c.1165_1167del	NP_060237.2:p.Phe389del
NM_130849.3:c.1240_1242del	NP_570901.2:p.Phe414del
XM_006716599.1:c.1240_1242del	XP_006716662.1:p.Phe414del
XM_011517153.1:c.958_960del	XP_011515455.1:p.Phe320del
XM_024447188.1:c.958_960del	XP_024302956.1:p.Phe320del
XM_024447189.1:c.958_960del	XP_024302957.1:p.Phe320del
NM_001374839.1:c.958_960del	NP_001361768.1:p.Phe320del
NM_017767.3:c.1165_1167del	NP_060237.3:p.Phe389del
NM_130849.4:c.1240_1242del MANE Select	NP_570901.3:p.Phe414del