Canonical Allele Identifier: CA2295937387
Gene: SLC39A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.36114075G= , CM000680.2:g.36114075G= GRCh38
NC_000018.9:g.33694038G= , CM000680.1:g.33694038G= GRCh37
NC_000018.8:g.31948036G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000269187.10:c.1843+22C= MANE Select ENSP00000269187.4:n.1843+22C=
ENST00000269187.9:c.1843+22C= ENSP00000269187.4:n.1843+22C=
ENST00000440549.6:c.1018+22C= ENSP00000401139.1:n.1018+22C=
ENST00000586829.1:c.544+22C= ENSP00000467724.1:n.544+22C=
ENST00000590986.5:c.1843+22C= ENSP00000465915.1:n.1843+22C=
NM_001099406.1:c.1018+22C= NP_001092876.1:n.1018+22C=
NM_012319.3:c.1843+22C= NP_036451.3:n.1843+22C=
XM_011525900.1:c.1843+22C= XP_011524202.1:n.1843+22C=
XM_011525901.1:c.1843+22C= XP_011524203.1:n.1843+22C=
XM_011525900.2:c.1843+22C= XP_011524202.1:n.1843+22C=
XM_011525901.2:c.1843+22C= XP_011524203.1:n.1843+22C=
NM_012319.4:c.1843+22C= MANE Select NP_036451.4:n.1843+22C=
NM_001099406.2:c.1018+22C= NP_001092876.1:n.1018+22C=