Canonical Allele Identifier: CA919964682

Gene: SLC39A6

Linked Data

• dbSNP Id: rs1598706113

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36114300_36114301insGTATA , CM000680.2:g.36114300_36114301insGTATA	GRCh38
NC_000018.9:g.33694263_33694264insGTATA , CM000680.1:g.33694263_33694264insGTATA	GRCh37
NC_000018.8:g.31948261_31948262insGTATA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269187.10:c.1639_1640insTATAC MANE Select	ENSP00000269187.4:p.Thr547IlefsTer?
ENST00000269187.9:c.1639_1640insTATAC	ENSP00000269187.4:p.Thr547IlefsTer?
ENST00000440549.6:c.814_815insTATAC	ENSP00000401139.1:p.Thr272IlefsTer?
ENST00000586829.1:c.340_341insTATAC	ENSP00000467724.1:p.Thr114IlefsTer?
ENST00000590986.5:c.1639_1640insTATAC	ENSP00000465915.1:p.Thr547IlefsTer?
NM_001099406.1:c.814_815insTATAC	NP_001092876.1:p.Thr272IlefsTer?
NM_012319.3:c.1639_1640insTATAC	NP_036451.3:p.Thr547IlefsTer?
XM_011525900.1:c.1639_1640insTATAC	XP_011524202.1:p.Thr547IlefsTer?
XM_011525901.1:c.1639_1640insTATAC	XP_011524203.1:p.Thr547IlefsTer?
XM_011525900.2:c.1639_1640insTATAC	XP_011524202.1:p.Thr547IlefsTer?
XM_011525901.2:c.1639_1640insTATAC	XP_011524203.1:p.Thr547IlefsTer?
NM_012319.4:c.1639_1640insTATAC MANE Select	NP_036451.4:p.Thr547IlefsTer?
NM_001099406.2:c.814_815insTATAC	NP_001092876.1:p.Thr272IlefsTer?