Canonical Allele Identifier: CA2689098723

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414342-T-TGGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414343_144414344insGGCG , CM000670.2:g.144414343_144414344insGGCG	GRCh38
NC_000008.10:g.145639727_145639728insGGCG , CM000670.1:g.145639727_145639728insGGCG	GRCh37
NC_000008.9:g.145610535_145610536insGGCG	NCBI36
NG_012234.2:g.7548_7549insGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1068_1069insGCCC MANE Select	ENSP00000301305.4:p.Thr357AlafsTer?
ENST00000276833.9:c.993_994insGCCC	ENSP00000276833.5:p.Thr332AlafsTer?
ENST00000301305.7:c.1068_1069insGCCC	ENSP00000301305.3:p.Thr357AlafsTer?
NM_017767.2:c.993_994insGCCC	NP_060237.2:p.Thr332AlafsTer?
NM_130849.3:c.1068_1069insGCCC	NP_570901.2:p.Thr357AlafsTer?
XM_006716599.1:c.1068_1069insGCCC	XP_006716662.1:p.Thr357AlafsTer?
XM_011517153.1:c.786_787insGCCC	XP_011515455.1:p.Thr263AlafsTer?
XM_024447188.1:c.786_787insGCCC	XP_024302956.1:p.Thr263AlafsTer?
XM_024447189.1:c.786_787insGCCC	XP_024302957.1:p.Thr263AlafsTer?
NM_001374839.1:c.786_787insGCCC	NP_001361768.1:p.Thr263AlafsTer?
NM_017767.3:c.993_994insGCCC	NP_060237.3:p.Thr332AlafsTer?
NM_130849.4:c.1068_1069insGCCC MANE Select	NP_570901.3:p.Thr357AlafsTer?