Canonical Allele Identifier: CA1826307002

Gene: SLC39A4

Linked Data

• dbSNP Id: rs1822056562
• gnomAD v4: 8-144414196-AGGGCACGGCCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414200_144414210del , CM000670.2:g.144414200_144414210del	GRCh38
NG_012234.2:g.7684_7694del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1149+55_1149+65del MANE Select	ENSP00000301305.4:n.1149+55_1149+65del
ENST00000276833.9:c.1074+55_1074+65del	ENSP00000276833.5:n.1074+55_1074+65del
ENST00000301305.7:c.1149+55_1149+65del	ENSP00000301305.3:n.1149+55_1149+65del
NM_017767.2:c.1074+55_1074+65del	NP_060237.2:n.1074+55_1074+65del
NM_130849.3:c.1149+55_1149+65del	NP_570901.2:n.1149+55_1149+65del
XM_006716599.1:c.1149+55_1149+65del	XP_006716662.1:n.1149+55_1149+65del
XM_011517153.1:c.867+55_867+65del	XP_011515455.1:n.867+55_867+65del
XM_024447188.1:c.867+55_867+65del	XP_024302956.1:n.867+55_867+65del
XM_024447189.1:c.867+55_867+65del	XP_024302957.1:n.867+55_867+65del
NM_001374839.1:c.867+55_867+65del	NP_001361768.1:n.867+55_867+65del
NM_017767.3:c.1074+55_1074+65del	NP_060237.3:n.1074+55_1074+65del
NM_130849.4:c.1149+55_1149+65del MANE Select	NP_570901.3:n.1149+55_1149+65del