Canonical Allele Identifier: CA2641520504
Gene: SLC39A6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.36114539del , CM000680.2:g.36114539del GRCh38
NC_000018.9:g.33694502del , CM000680.1:g.33694502del GRCh37
NC_000018.8:g.31948500del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269187.10:c.1466-63del MANE Select ENSP00000269187.4:n.1466-63del
ENST00000269187.9:c.1466-63del ENSP00000269187.4:n.1466-63del
ENST00000440549.6:c.641-63del ENSP00000401139.1:n.641-63del
ENST00000586829.1:c.167-63del ENSP00000467724.1:n.167-63del
ENST00000590986.5:c.1466-63del ENSP00000465915.1:n.1466-63del
NM_001099406.1:c.641-63del NP_001092876.1:n.641-63del
NM_012319.3:c.1466-63del NP_036451.3:n.1466-63del
XM_011525900.1:c.1466-63del XP_011524202.1:n.1466-63del
XM_011525901.1:c.1466-63del XP_011524203.1:n.1466-63del
XM_011525900.2:c.1466-63del XP_011524202.1:n.1466-63del
XM_011525901.2:c.1466-63del XP_011524203.1:n.1466-63del
NM_012319.4:c.1466-63del MANE Select NP_036451.4:n.1466-63del
NM_001099406.2:c.641-63del NP_001092876.1:n.641-63del