Canonical Allele Identifier: CA372619659

Gene: SLC39A4

Linked Data

• MyVariant Identifiers: chr8:g.145639371A>T (hg19) ; chr8:g.144413987A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144413987A>T , CM000670.2:g.144413987A>T	GRCh38
NC_000008.10:g.145639371A>T , CM000670.1:g.145639371A>T	GRCh37
NC_000008.9:g.145610179A>T	NCBI36
NG_012234.2:g.7904T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1258T>A MANE Select	ENSP00000301305.4:p.Phe420Ile
ENST00000276833.9:c.1183T>A	ENSP00000276833.5:p.Phe395Ile
ENST00000301305.7:c.1258T>A	ENSP00000301305.3:p.Phe420Ile
ENST00000531789.1:n.95T>A
NM_017767.2:c.1183T>A	NP_060237.2:p.Phe395Ile
NM_130849.3:c.1258T>A	NP_570901.2:p.Phe420Ile
XM_006716599.1:c.1258T>A	XP_006716662.1:p.Phe420Ile
XM_011517153.1:c.976T>A	XP_011515455.1:p.Phe326Ile
XM_024447188.1:c.976T>A	XP_024302956.1:p.Phe326Ile
XM_024447189.1:c.976T>A	XP_024302957.1:p.Phe326Ile
NM_001374839.1:c.976T>A	NP_001361768.1:p.Phe326Ile
NM_017767.3:c.1183T>A	NP_060237.3:p.Phe395Ile
NM_130849.4:c.1258T>A MANE Select	NP_570901.3:p.Phe420Ile