Canonical Allele Identifier: CA10630457

Gene: SLC39A4

Linked Data

• ClinVar Variation Id: 362237
• ClinVar RCV Id: RCV000336853
• dbSNP Id: rs886062747
• MyVariant Identifiers: chr8:g.145639479C>T (hg19) ; chr8:g.144414095C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414095C>T , CM000670.2:g.144414095C>T	GRCh38
NC_000008.10:g.145639479C>T , CM000670.1:g.145639479C>T	GRCh37
NC_000008.9:g.145610287C>T	NCBI36
NG_012234.2:g.7796G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1150G>A MANE Select	ENSP00000301305.4:p.Val384Met
ENST00000276833.9:c.1075G>A	ENSP00000276833.5:p.Val359Met
ENST00000301305.7:c.1150G>A	ENSP00000301305.3:p.Val384Met
NM_017767.2:c.1075G>A	NP_060237.2:p.Val359Met
NM_130849.3:c.1150G>A	NP_570901.2:p.Val384Met
XM_006716599.1:c.1150G>A	XP_006716662.1:p.Val384Met
XM_011517153.1:c.868G>A	XP_011515455.1:p.Val290Met
XM_024447188.1:c.868G>A	XP_024302956.1:p.Val290Met
XM_024447189.1:c.868G>A	XP_024302957.1:p.Val290Met
NM_001374839.1:c.868G>A	NP_001361768.1:p.Val290Met
NM_017767.3:c.1075G>A	NP_060237.3:p.Val359Met
NM_130849.4:c.1150G>A MANE Select	NP_570901.3:p.Val384Met