Canonical Allele Identifier: CA1826307102

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414342T= , CM000670.2:g.144414342T=	GRCh38
NC_000008.10:g.145639726T= , CM000670.1:g.145639726T=	GRCh37
NC_000008.9:g.145610534T=	NCBI36
NG_012234.2:g.7549A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1069A= MANE Select	ENSP00000301305.4:p.Thr357=
ENST00000276833.9:c.994A=	ENSP00000276833.5:p.Thr332=
ENST00000301305.7:c.1069A=	ENSP00000301305.3:p.Thr357=
NM_017767.2:c.994A=	NP_060237.2:p.Thr332=
NM_130849.3:c.1069A=	NP_570901.2:p.Thr357=
XM_006716599.1:c.1069A=	XP_006716662.1:p.Thr357=
XM_011517153.1:c.787A=	XP_011515455.1:p.Thr263=
XM_024447188.1:c.787A=	XP_024302956.1:p.Thr263=
XM_024447189.1:c.787A=	XP_024302957.1:p.Thr263=
NM_001374839.1:c.787A=	NP_001361768.1:p.Thr263=
NM_017767.3:c.994A=	NP_060237.3:p.Thr332=
NM_130849.4:c.1069A= MANE Select	NP_570901.3:p.Thr357=