Canonical Allele Identifier: CA2689098973

Gene: SLC39A4

Linked Data

• ClinVar Variation Id: 2707762
• ClinVar RCV Id: RCV003545022
• gnomAD v4: 8-144414436-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414441dup , CM000670.2:g.144414441dup	GRCh38
NC_000008.10:g.145639825dup , CM000670.1:g.145639825dup	GRCh37
NC_000008.9:g.145610633dup	NCBI36
NG_012234.2:g.7454dup

Transcript Alleles

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