Canonical Allele Identifier: CA2689098548

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414315-TCAGGAAGGTCTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414321_144414332del , CM000670.2:g.144414321_144414332del	GRCh38
NC_000008.10:g.145639705_145639716del , CM000670.1:g.145639705_145639716del	GRCh37
NC_000008.9:g.145610513_145610524del	NCBI36
NG_012234.2:g.7564_7575del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1084_1095del MANE Select	ENSP00000301305.4:p.Gln362_Leu365del
ENST00000276833.9:c.1009_1020del	ENSP00000276833.5:p.Gln337_Leu340del
ENST00000301305.7:c.1084_1095del	ENSP00000301305.3:p.Gln362_Leu365del
NM_017767.2:c.1009_1020del	NP_060237.2:p.Gln337_Leu340del
NM_130849.3:c.1084_1095del	NP_570901.2:p.Gln362_Leu365del
XM_006716599.1:c.1084_1095del	XP_006716662.1:p.Gln362_Leu365del
XM_011517153.1:c.802_813del	XP_011515455.1:p.Gln268_Leu271del
XM_024447188.1:c.802_813del	XP_024302956.1:p.Gln268_Leu271del
XM_024447189.1:c.802_813del	XP_024302957.1:p.Gln268_Leu271del
NM_001374839.1:c.802_813del	NP_001361768.1:p.Gln268_Leu271del
NM_017767.3:c.1009_1020del	NP_060237.3:p.Gln337_Leu340del
NM_130849.4:c.1084_1095del MANE Select	NP_570901.3:p.Gln362_Leu365del