Canonical Allele Identifier: CA2689097752

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414073-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414079_144414080del , CM000670.2:g.144414079_144414080del	GRCh38
NC_000008.10:g.145639463_145639464del , CM000670.1:g.145639463_145639464del	GRCh37
NC_000008.9:g.145610271_145610272del	NCBI36
NG_012234.2:g.7816_7817del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1170_1171del MANE Select	ENSP00000301305.4:p.His390GlnfsTer27
ENST00000276833.9:c.1095_1096del	ENSP00000276833.5:p.His365GlnfsTer27
ENST00000301305.7:c.1170_1171del	ENSP00000301305.3:p.His390GlnfsTer27
ENST00000531789.1:n.7_8del
NM_017767.2:c.1095_1096del	NP_060237.2:p.His365GlnfsTer27
NM_130849.3:c.1170_1171del	NP_570901.2:p.His390GlnfsTer27
XM_006716599.1:c.1170_1171del	XP_006716662.1:p.His390GlnfsTer27
XM_011517153.1:c.888_889del	XP_011515455.1:p.His296GlnfsTer27
XM_024447188.1:c.888_889del	XP_024302956.1:p.His296GlnfsTer27
XM_024447189.1:c.888_889del	XP_024302957.1:p.His296GlnfsTer27
NM_001374839.1:c.888_889del	NP_001361768.1:p.His296GlnfsTer27
NM_017767.3:c.1095_1096del	NP_060237.3:p.His365GlnfsTer27
NM_130849.4:c.1170_1171del MANE Select	NP_570901.3:p.His390GlnfsTer27