Canonical Allele Identifier: CA463449656

Gene: SLC39A4

Linked Data

• ClinVar Variation Id: 2839149
• ClinVar RCV Id: RCV003723319
• dbSNP Id: rs1554872997
• gnomAD v2: 8-145639724-G-T
• gnomAD v4: 8-144414340-G-T
• MyVariant Identifiers: chr8:g.145639724G>T (hg19) ; chr8:g.144414340G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414340G>T , CM000670.2:g.144414340G>T	GRCh38
NC_000008.10:g.145639724G>T , CM000670.1:g.145639724G>T	GRCh37
NC_000008.9:g.145610532G>T	NCBI36
NG_012234.2:g.7551C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1071C>A MANE Select	ENSP00000301305.4:p.Thr357=
ENST00000276833.9:c.996C>A	ENSP00000276833.5:p.Thr332=
ENST00000301305.7:c.1071C>A	ENSP00000301305.3:p.Thr357=
NM_017767.2:c.996C>A	NP_060237.2:p.Thr332=
NM_130849.3:c.1071C>A	NP_570901.2:p.Thr357=
XM_006716599.1:c.1071C>A	XP_006716662.1:p.Thr357=
XM_011517153.1:c.789C>A	XP_011515455.1:p.Thr263=
XM_024447188.1:c.789C>A	XP_024302956.1:p.Thr263=
XM_024447189.1:c.789C>A	XP_024302957.1:p.Thr263=
NM_001374839.1:c.789C>A	NP_001361768.1:p.Thr263=
NM_017767.3:c.996C>A	NP_060237.3:p.Thr332=
NM_130849.4:c.1071C>A MANE Select	NP_570901.3:p.Thr357=