Canonical Allele Identifier: CA2689097763

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414080-TATGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414082_144414085del , CM000670.2:g.144414082_144414085del	GRCh38
NC_000008.10:g.145639466_145639469del , CM000670.1:g.145639466_145639469del	GRCh37
NC_000008.9:g.145610274_145610277del	NCBI36
NG_012234.2:g.7807_7810del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1161_1164del MANE Select	ENSP00000301305.4:p.His390AlafsTer?
ENST00000276833.9:c.1086_1089del	ENSP00000276833.5:p.His365AlafsTer?
ENST00000301305.7:c.1161_1164del	ENSP00000301305.3:p.His390AlafsTer?
NM_017767.2:c.1086_1089del	NP_060237.2:p.His365AlafsTer?
NM_130849.3:c.1161_1164del	NP_570901.2:p.His390AlafsTer?
XM_006716599.1:c.1161_1164del	XP_006716662.1:p.His390AlafsTer?
XM_011517153.1:c.879_882del	XP_011515455.1:p.His296AlafsTer?
XM_024447188.1:c.879_882del	XP_024302956.1:p.His296AlafsTer?
XM_024447189.1:c.879_882del	XP_024302957.1:p.His296AlafsTer?
NM_001374839.1:c.879_882del	NP_001361768.1:p.His296AlafsTer?
NM_017767.3:c.1086_1089del	NP_060237.3:p.His365AlafsTer?
NM_130849.4:c.1161_1164del MANE Select	NP_570901.3:p.His390AlafsTer?