Canonical Allele Identifier: CA2295937419
Gene: SLC39A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.36114166C= , CM000680.2:g.36114166C= GRCh38
NC_000018.9:g.33694129C= , CM000680.1:g.33694129C= GRCh37
NC_000018.8:g.31948127C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000269187.10:c.1774G= MANE Select ENSP00000269187.4:p.Val592=
ENST00000269187.9:c.1774G= ENSP00000269187.4:p.Val592=
ENST00000440549.6:c.949G= ENSP00000401139.1:p.Val317=
ENST00000586829.1:c.475G= ENSP00000467724.1:p.Val159=
ENST00000590986.5:c.1774G= ENSP00000465915.1:p.Val592=
NM_001099406.1:c.949G= NP_001092876.1:p.Val317=
NM_012319.3:c.1774G= NP_036451.3:p.Val592=
XM_011525900.1:c.1774G= XP_011524202.1:p.Val592=
XM_011525901.1:c.1774G= XP_011524203.1:p.Val592=
XM_011525900.2:c.1774G= XP_011524202.1:p.Val592=
XM_011525901.2:c.1774G= XP_011524203.1:p.Val592=
NM_012319.4:c.1774G= MANE Select NP_036451.4:p.Val592=
NM_001099406.2:c.949G= NP_001092876.1:p.Val317=