Canonical Allele Identifier: CA2689097937

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414129-TCCCAGGGCGCCTCCCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414132_144414147del , CM000670.2:g.144414132_144414147del	GRCh38
NG_012234.2:g.7746_7761del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1150-50_1150-35del MANE Select	ENSP00000301305.4:n.1150-50_1150-35del
ENST00000276833.9:c.1075-50_1075-35del	ENSP00000276833.5:n.1075-50_1075-35del
ENST00000301305.7:c.1150-50_1150-35del	ENSP00000301305.3:n.1150-50_1150-35del
NM_017767.2:c.1075-50_1075-35del	NP_060237.2:n.1075-50_1075-35del
NM_130849.3:c.1150-50_1150-35del	NP_570901.2:n.1150-50_1150-35del
XM_006716599.1:c.1150-50_1150-35del	XP_006716662.1:n.1150-50_1150-35del
XM_011517153.1:c.868-50_868-35del	XP_011515455.1:n.868-50_868-35del
XM_024447188.1:c.868-50_868-35del	XP_024302956.1:n.868-50_868-35del
XM_024447189.1:c.868-50_868-35del	XP_024302957.1:n.868-50_868-35del
NM_001374839.1:c.868-50_868-35del	NP_001361768.1:n.868-50_868-35del
NM_017767.3:c.1075-50_1075-35del	NP_060237.3:n.1075-50_1075-35del
NM_130849.4:c.1150-50_1150-35del MANE Select	NP_570901.3:n.1150-50_1150-35del