Canonical Allele Identifier: CA4941445

Gene: SLC39A4

Linked Data

• dbSNP Id: rs782791177
• ExAC: 8:145639867 CCTGCTTCCCGGGCG / C
• gnomAD v2: 8-145639867-CCTGCTTCCCGGGCG-C
• gnomAD v4: 8-144414483-CCTGCTTCCCGGGCG-C
• MyVariant Identifiers: chr8:g.145639868_145639881del (hg19) ; chr8:g.144414484_144414497del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414489_144414502del , CM000670.2:g.144414489_144414502del	GRCh38
NC_000008.10:g.145639873_145639886del , CM000670.1:g.145639873_145639886del	GRCh37
NC_000008.9:g.145610681_145610694del	NCBI36
NG_012234.2:g.7394_7407del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.977-63_977-50del MANE Select	ENSP00000301305.4:n.977-63_977-50del
ENST00000276833.9:c.902-63_902-50del	ENSP00000276833.5:n.902-63_902-50del
ENST00000301305.7:c.977-63_977-50del	ENSP00000301305.3:n.977-63_977-50del
NM_017767.2:c.902-63_902-50del	NP_060237.2:n.902-63_902-50del
NM_130849.3:c.977-63_977-50del	NP_570901.2:n.977-63_977-50del
XM_006716599.1:c.977-63_977-50del	XP_006716662.1:n.977-63_977-50del
XM_011517153.1:c.695-63_695-50del	XP_011515455.1:n.695-63_695-50del
XM_024447188.1:c.695-63_695-50del	XP_024302956.1:n.695-63_695-50del
XM_024447189.1:c.695-63_695-50del	XP_024302957.1:n.695-63_695-50del
NM_001374839.1:c.695-63_695-50del	NP_001361768.1:n.695-63_695-50del
NM_017767.3:c.902-63_902-50del	NP_060237.3:n.902-63_902-50del
NM_130849.4:c.977-63_977-50del MANE Select	NP_570901.3:n.977-63_977-50del