Canonical Allele Identifier: CA586164216

Gene: SLC39A4

Linked Data

• dbSNP Id: rs1166496067
• gnomAD v2: 8-145639545-AG-A
• gnomAD v3: 8-144414161-AG-A
• gnomAD v4: 8-144414161-AG-A
• MyVariant Identifiers: chr8:g.145639546del (hg19) ; chr8:g.144414162del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414165del , CM000670.2:g.144414165del	GRCh38
NC_000008.10:g.145639549del , CM000670.1:g.145639549del	GRCh37
NC_000008.9:g.145610357del	NCBI36
NG_012234.2:g.7729del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1150-67del MANE Select	ENSP00000301305.4:n.1150-67del
ENST00000276833.9:c.1075-67del	ENSP00000276833.5:n.1075-67del
ENST00000301305.7:c.1150-67del	ENSP00000301305.3:n.1150-67del
NM_017767.2:c.1075-67del	NP_060237.2:n.1075-67del
NM_130849.3:c.1150-67del	NP_570901.2:n.1150-67del
XM_006716599.1:c.1150-67del	XP_006716662.1:n.1150-67del
XM_011517153.1:c.868-67del	XP_011515455.1:n.868-67del
XM_024447188.1:c.868-67del	XP_024302956.1:n.868-67del
XM_024447189.1:c.868-67del	XP_024302957.1:n.868-67del
NM_001374839.1:c.868-67del	NP_001361768.1:n.868-67del
NM_017767.3:c.1075-67del	NP_060237.3:n.1075-67del
NM_130849.4:c.1150-67del MANE Select	NP_570901.3:n.1150-67del