Canonical Allele Identifier: CA4941436

Gene: SLC39A4

Linked Data

• ClinVar Variation Id: 1095388
• ClinVar RCV Id: RCV001416281
• dbSNP Id: rs782070713
• ExAC: 8:145639826 C / T
• gnomAD v2: 8-145639826-C-T
• gnomAD v3: 8-144414442-C-T
• gnomAD v4: 8-144414442-C-T
• MyVariant Identifiers: chr8:g.145639826C>T (hg19) ; chr8:g.144414442C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414442C>T , CM000670.2:g.144414442C>T	GRCh38
NC_000008.10:g.145639826C>T , CM000670.1:g.145639826C>T	GRCh37
NC_000008.9:g.145610634C>T	NCBI36
NG_012234.2:g.7449G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.977-8G>A MANE Select	ENSP00000301305.4:n.977-8G>A
ENST00000276833.9:c.902-8G>A	ENSP00000276833.5:n.902-8G>A
ENST00000301305.7:c.977-8G>A	ENSP00000301305.3:n.977-8G>A
NM_017767.2:c.902-8G>A	NP_060237.2:n.902-8G>A
NM_130849.3:c.977-8G>A	NP_570901.2:n.977-8G>A
XM_006716599.1:c.977-8G>A	XP_006716662.1:n.977-8G>A
XM_011517153.1:c.695-8G>A	XP_011515455.1:n.695-8G>A
XM_024447188.1:c.695-8G>A	XP_024302956.1:n.695-8G>A
XM_024447189.1:c.695-8G>A	XP_024302957.1:n.695-8G>A
NM_001374839.1:c.695-8G>A	NP_001361768.1:n.695-8G>A
NM_017767.3:c.902-8G>A	NP_060237.3:n.902-8G>A
NM_130849.4:c.977-8G>A MANE Select	NP_570901.3:n.977-8G>A