Canonical Allele Identifier: CA1826307137

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414395_144414398delinsAGGC , CM000670.2:g.144414395_144414398delinsAGGC	GRCh38
NC_000008.10:g.145639779_145639782delinsAGGC , CM000670.1:g.145639779_145639782delinsAGGC	GRCh37
NC_000008.9:g.145610587_145610590delinsAGGC	NCBI36
NG_012234.2:g.7493_7496delinsGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1013_1016delinsGCCT MANE Select	ENSP00000301305.4:p.Cys338=
ENST00000276833.9:c.938_941delinsGCCT	ENSP00000276833.5:p.Cys313=
ENST00000301305.7:c.1013_1016delinsGCCT	ENSP00000301305.3:p.Cys338=
NM_017767.2:c.938_941delinsGCCT	NP_060237.2:p.Cys313=
NM_130849.3:c.1013_1016delinsGCCT	NP_570901.2:p.Cys338=
XM_006716599.1:c.1013_1016delinsGCCT	XP_006716662.1:p.Cys338=
XM_011517153.1:c.731_734delinsGCCT	XP_011515455.1:p.Cys244=
XM_024447188.1:c.731_734delinsGCCT	XP_024302956.1:p.Cys244=
XM_024447189.1:c.731_734delinsGCCT	XP_024302957.1:p.Cys244=
NM_001374839.1:c.731_734delinsGCCT	NP_001361768.1:p.Cys244=
NM_017767.3:c.938_941delinsGCCT	NP_060237.3:p.Cys313=
NM_130849.4:c.1013_1016delinsGCCT MANE Select	NP_570901.3:p.Cys338=