Canonical Allele Identifier: CA2549671254

Gene: SLC39A6

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36114394_36114395insATA , CM000680.2:g.36114394_36114395insATA	GRCh38
NC_000018.9:g.33694357_33694358insATA , CM000680.1:g.33694357_33694358insATA	GRCh37
NC_000018.8:g.31948355_31948356insATA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269187.10:c.1545_1546insTAT MANE Select	ENSP00000269187.4:p.Glu515_Glu516insTyr
ENST00000269187.9:c.1545_1546insTAT	ENSP00000269187.4:p.Glu515_Glu516insTyr
ENST00000440549.6:c.720_721insTAT	ENSP00000401139.1:p.Glu240_Glu241insTyr
ENST00000586829.1:c.246_247insTAT	ENSP00000467724.1:p.Glu82_Glu83insTyr
ENST00000590986.5:c.1545_1546insTAT	ENSP00000465915.1:p.Glu515_Glu516insTyr
NM_001099406.1:c.720_721insTAT	NP_001092876.1:p.Glu240_Glu241insTyr
NM_012319.3:c.1545_1546insTAT	NP_036451.3:p.Glu515_Glu516insTyr
XM_011525900.1:c.1545_1546insTAT	XP_011524202.1:p.Glu515_Glu516insTyr
XM_011525901.1:c.1545_1546insTAT	XP_011524203.1:p.Glu515_Glu516insTyr
XM_011525900.2:c.1545_1546insTAT	XP_011524202.1:p.Glu515_Glu516insTyr
XM_011525901.2:c.1545_1546insTAT	XP_011524203.1:p.Glu515_Glu516insTyr
NM_012319.4:c.1545_1546insTAT MANE Select	NP_036451.4:p.Glu515_Glu516insTyr
NM_001099406.2:c.720_721insTAT	NP_001092876.1:p.Glu240_Glu241insTyr