Canonical Allele Identifier: CA1826306877

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144413998A= , CM000670.2:g.144413998A=	GRCh38
NC_000008.10:g.145639382A= , CM000670.1:g.145639382A=	GRCh37
NC_000008.9:g.145610190A=	NCBI36
NG_012234.2:g.7893T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1247T= MANE Select	ENSP00000301305.4:p.Phe416=
ENST00000276833.9:c.1172T=	ENSP00000276833.5:p.Phe391=
ENST00000301305.7:c.1247T=	ENSP00000301305.3:p.Phe416=
ENST00000531789.1:n.84T=
NM_017767.2:c.1172T=	NP_060237.2:p.Phe391=
NM_130849.3:c.1247T=	NP_570901.2:p.Phe416=
XM_006716599.1:c.1247T=	XP_006716662.1:p.Phe416=
XM_011517153.1:c.965T=	XP_011515455.1:p.Phe322=
XM_024447188.1:c.965T=	XP_024302956.1:p.Phe322=
XM_024447189.1:c.965T=	XP_024302957.1:p.Phe322=
NM_001374839.1:c.965T=	NP_001361768.1:p.Phe322=
NM_017767.3:c.1172T=	NP_060237.3:p.Phe391=
NM_130849.4:c.1247T= MANE Select	NP_570901.3:p.Phe416=