Canonical Allele Identifier: CA4941316

Gene: SLC39A4

Linked Data

• ClinVar Variation Id: 1606784
• ClinVar RCV Id: RCV002162511
• dbSNP Id: rs782243870
• ExAC: 8:145639369 G / A
• gnomAD v2: 8-145639369-G-A
• gnomAD v4: 8-144413985-G-A
• MyVariant Identifiers: chr8:g.145639369G>A (hg19) ; chr8:g.144413985G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144413985G>A , CM000670.2:g.144413985G>A	GRCh38
NC_000008.10:g.145639369G>A , CM000670.1:g.145639369G>A	GRCh37
NC_000008.9:g.145610177G>A	NCBI36
NG_012234.2:g.7906C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1260C>T MANE Select	ENSP00000301305.4:p.Phe420=
ENST00000276833.9:c.1185C>T	ENSP00000276833.5:p.Phe395=
ENST00000301305.7:c.1260C>T	ENSP00000301305.3:p.Phe420=
ENST00000531789.1:n.97C>T
NM_017767.2:c.1185C>T	NP_060237.2:p.Phe395=
NM_130849.3:c.1260C>T	NP_570901.2:p.Phe420=
XM_006716599.1:c.1260C>T	XP_006716662.1:p.Phe420=
XM_011517153.1:c.978C>T	XP_011515455.1:p.Phe326=
XM_024447188.1:c.978C>T	XP_024302956.1:p.Phe326=
XM_024447189.1:c.978C>T	XP_024302957.1:p.Phe326=
NM_001374839.1:c.978C>T	NP_001361768.1:p.Phe326=
NM_017767.3:c.1185C>T	NP_060237.3:p.Phe395=
NM_130849.4:c.1260C>T MANE Select	NP_570901.3:p.Phe420=