Canonical Allele Identifier: CA402205335
Gene: SLC39A6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.36114303T>G , CM000680.2:g.36114303T>G GRCh38
NC_000018.9:g.33694266T>G , CM000680.1:g.33694266T>G GRCh37
NC_000018.8:g.31948264T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269187.10:c.1637A>C MANE Select ENSP00000269187.4:p.Asp546Ala
ENST00000269187.9:c.1637A>C ENSP00000269187.4:p.Asp546Ala
ENST00000440549.6:c.812A>C ENSP00000401139.1:p.Asp271Ala
ENST00000586829.1:c.338A>C ENSP00000467724.1:p.Asp113Ala
ENST00000590986.5:c.1637A>C ENSP00000465915.1:p.Asp546Ala
NM_001099406.1:c.812A>C NP_001092876.1:p.Asp271Ala
NM_012319.3:c.1637A>C NP_036451.3:p.Asp546Ala
XM_011525900.1:c.1637A>C XP_011524202.1:p.Asp546Ala
XM_011525901.1:c.1637A>C XP_011524203.1:p.Asp546Ala
XM_011525900.2:c.1637A>C XP_011524202.1:p.Asp546Ala
XM_011525901.2:c.1637A>C XP_011524203.1:p.Asp546Ala
NM_012319.4:c.1637A>C MANE Select NP_036451.4:p.Asp546Ala
NM_001099406.2:c.812A>C NP_001092876.1:p.Asp271Ala