Canonical Allele Identifier: CA2689098692

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414340-G-GTA

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414340_144414341insTA , CM000670.2:g.144414340_144414341insTA	GRCh38
NC_000008.10:g.145639724_145639725insTA , CM000670.1:g.145639724_145639725insTA	GRCh37
NC_000008.9:g.145610532_145610533insTA	NCBI36
NG_012234.2:g.7550_7551insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1070_1071insTA MANE Select	ENSP00000301305.4:p.His358ThrfsTer9
ENST00000276833.9:c.995_996insTA	ENSP00000276833.5:p.His333ThrfsTer9
ENST00000301305.7:c.1070_1071insTA	ENSP00000301305.3:p.His358ThrfsTer9
NM_017767.2:c.995_996insTA	NP_060237.2:p.His333ThrfsTer9
NM_130849.3:c.1070_1071insTA	NP_570901.2:p.His358ThrfsTer9
XM_006716599.1:c.1070_1071insTA	XP_006716662.1:p.His358ThrfsTer9
XM_011517153.1:c.788_789insTA	XP_011515455.1:p.His264ThrfsTer9
XM_024447188.1:c.788_789insTA	XP_024302956.1:p.His264ThrfsTer9
XM_024447189.1:c.788_789insTA	XP_024302957.1:p.His264ThrfsTer9
NM_001374839.1:c.788_789insTA	NP_001361768.1:p.His264ThrfsTer9
NM_017767.3:c.995_996insTA	NP_060237.3:p.His333ThrfsTer9
NM_130849.4:c.1070_1071insTA MANE Select	NP_570901.3:p.His358ThrfsTer9