Canonical Allele Identifier: CA1826306882

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414005_144414006delinsAG , CM000670.2:g.144414005_144414006delinsAG	GRCh38
NC_000008.10:g.145639389_145639390delinsAG , CM000670.1:g.145639389_145639390delinsAG	GRCh37
NC_000008.9:g.145610197_145610198delinsAG	NCBI36
NG_012234.2:g.7885_7886delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1239_1240delinsCT MANE Select	ENSP00000301305.4:p.Phe413=
ENST00000276833.9:c.1164_1165delinsCT	ENSP00000276833.5:p.Phe388=
ENST00000301305.7:c.1239_1240delinsCT	ENSP00000301305.3:p.Phe413=
ENST00000531789.1:n.76_77delinsCT
NM_017767.2:c.1164_1165delinsCT	NP_060237.2:p.Phe388=
NM_130849.3:c.1239_1240delinsCT	NP_570901.2:p.Phe413=
XM_006716599.1:c.1239_1240delinsCT	XP_006716662.1:p.Phe413=
XM_011517153.1:c.957_958delinsCT	XP_011515455.1:p.Phe319=
XM_024447188.1:c.957_958delinsCT	XP_024302956.1:p.Phe319=
XM_024447189.1:c.957_958delinsCT	XP_024302957.1:p.Phe319=
NM_001374839.1:c.957_958delinsCT	NP_001361768.1:p.Phe319=
NM_017767.3:c.1164_1165delinsCT	NP_060237.3:p.Phe388=
NM_130849.4:c.1239_1240delinsCT MANE Select	NP_570901.3:p.Phe413=