Canonical Allele Identifier: CA1826306886

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414011C= , CM000670.2:g.144414011C=	GRCh38
NC_000008.10:g.145639395C= , CM000670.1:g.145639395C=	GRCh37
NC_000008.9:g.145610203C=	NCBI36
NG_012234.2:g.7880G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1234G= MANE Select	ENSP00000301305.4:p.Ala412=
ENST00000276833.9:c.1159G=	ENSP00000276833.5:p.Ala387=
ENST00000301305.7:c.1234G=	ENSP00000301305.3:p.Ala412=
ENST00000531789.1:n.71G=
NM_017767.2:c.1159G=	NP_060237.2:p.Ala387=
NM_130849.3:c.1234G=	NP_570901.2:p.Ala412=
XM_006716599.1:c.1234G=	XP_006716662.1:p.Ala412=
XM_011517153.1:c.952G=	XP_011515455.1:p.Ala318=
XM_024447188.1:c.952G=	XP_024302956.1:p.Ala318=
XM_024447189.1:c.952G=	XP_024302957.1:p.Ala318=
NM_001374839.1:c.952G=	NP_001361768.1:p.Ala318=
NM_017767.3:c.1159G=	NP_060237.3:p.Ala387=
NM_130849.4:c.1234G= MANE Select	NP_570901.3:p.Ala412=