Canonical Allele Identifier: CA2295937527

Gene: SLC39A6

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36114451C= , CM000680.2:g.36114451C=	GRCh38
NC_000018.9:g.33694414C= , CM000680.1:g.33694414C=	GRCh37
NC_000018.8:g.31948412C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269187.10:c.1489G= MANE Select	ENSP00000269187.4:p.Asp497=
ENST00000269187.9:c.1489G=	ENSP00000269187.4:p.Asp497=
ENST00000440549.6:c.664G=	ENSP00000401139.1:p.Asp222=
ENST00000586829.1:c.190G=	ENSP00000467724.1:p.Asp64=
ENST00000590986.5:c.1489G=	ENSP00000465915.1:p.Asp497=
NM_001099406.1:c.664G=	NP_001092876.1:p.Asp222=
NM_012319.3:c.1489G=	NP_036451.3:p.Asp497=
XM_011525900.1:c.1489G=	XP_011524202.1:p.Asp497=
XM_011525901.1:c.1489G=	XP_011524203.1:p.Asp497=
XM_011525900.2:c.1489G=	XP_011524202.1:p.Asp497=
XM_011525901.2:c.1489G=	XP_011524203.1:p.Asp497=
NM_012319.4:c.1489G= MANE Select	NP_036451.4:p.Asp497=
NM_001099406.2:c.664G=	NP_001092876.1:p.Asp222=