Canonical Allele Identifier: CA463449499

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144413562C>G , CM000670.2:g.144413562C>G	GRCh38
NC_000008.10:g.145638946C>G , CM000670.1:g.145638946C>G	GRCh37
NC_000008.9:g.145609754C>G	NCBI36
NG_012234.2:g.8329G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_130849.4:c.1425G>C MANE Select	NP_570901.3:p.Ala475=
ENST00000301305.8:c.1425G>C MANE Select	ENSP00000301305.4:p.Ala475=
NM_001280557.1:c.-70G>C	NP_001267486.1:n.-70G>C
NM_001280557.2:c.-70G>C	NP_001267486.1:n.-70G>C
NM_001374839.1:c.1143G>C	NP_001361768.1:p.Ala381=
NM_017767.2:c.1350G>C	NP_060237.2:p.Ala450=
NM_017767.3:c.1350G>C	NP_060237.3:p.Ala450=
NM_130849.3:c.1425G>C	NP_570901.2:p.Ala475=
ENST00000276833.9:c.1350G>C	ENSP00000276833.5:p.Ala450=
ENST00000301305.7:c.1425G>C	ENSP00000301305.3:p.Ala475=
ENST00000527148.5:n.10G>C
ENST00000529462.5:n.24G>C
ENST00000530807.5:n.8G>C
ENST00000531013.1:n.30G>C
ENST00000531789.1:n.262G>C
ENST00000532718.5:n.25G>C
XM_006716599.1:c.1425G>C	XP_006716662.1:p.Ala475=
XM_011517153.1:c.1143G>C	XP_011515455.1:p.Ala381=
XM_024447188.1:c.1143G>C	XP_024302956.1:p.Ala381=
XM_024447189.1:c.1143G>C	XP_024302957.1:p.Ala381=