Canonical Allele Identifier: CA919964681

Gene: SLC39A6

Linked Data

• dbSNP Id: rs1598706109

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36114298_36114299insCAAT , CM000680.2:g.36114298_36114299insCAAT	GRCh38
NC_000018.9:g.33694261_33694262insCAAT , CM000680.1:g.33694261_33694262insCAAT	GRCh37
NC_000018.8:g.31948259_31948260insCAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269187.10:c.1641_1642insATTG MANE Select	ENSP00000269187.4:p.Leu548IlefsTer14
ENST00000269187.9:c.1641_1642insATTG	ENSP00000269187.4:p.Leu548IlefsTer14
ENST00000440549.6:c.816_817insATTG	ENSP00000401139.1:p.Leu273IlefsTer14
ENST00000586829.1:c.342_343insATTG	ENSP00000467724.1:p.Leu115IlefsTer14
ENST00000590986.5:c.1641_1642insATTG	ENSP00000465915.1:p.Leu548IlefsTer14
NM_001099406.1:c.816_817insATTG	NP_001092876.1:p.Leu273IlefsTer14
NM_012319.3:c.1641_1642insATTG	NP_036451.3:p.Leu548IlefsTer14
XM_011525900.1:c.1641_1642insATTG	XP_011524202.1:p.Leu548IlefsTer14
XM_011525901.1:c.1641_1642insATTG	XP_011524203.1:p.Leu548IlefsTer14
XM_011525900.2:c.1641_1642insATTG	XP_011524202.1:p.Leu548IlefsTer14
XM_011525901.2:c.1641_1642insATTG	XP_011524203.1:p.Leu548IlefsTer14
NM_012319.4:c.1641_1642insATTG MANE Select	NP_036451.4:p.Leu548IlefsTer14
NM_001099406.2:c.816_817insATTG	NP_001092876.1:p.Leu273IlefsTer14