Canonical Allele Identifier: CA4941399

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414297C= , CM000670.2:g.144414297C=	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1114G= MANE Select	ENSP00000301305.4:p.Val372=
ENST00000276833.9:c.1039G=	ENSP00000276833.5:p.Val347=
ENST00000301305.7:c.1114G=	ENSP00000301305.3:p.Val372=
XM_006716599.1:c.1114G=	XP_006716662.1:p.Val372=
XM_011517153.1:c.832G=	XP_011515455.1:p.Val278=
XM_024447188.1:c.832G=	XP_024302956.1:p.Val278=
XM_024447189.1:c.832G=	XP_024302957.1:p.Val278=
NM_001374839.1:c.832G=	NP_001361768.1:p.Val278=
NM_017767.3:c.1039G=	NP_060237.3:p.Val347=
NM_130849.4:c.1114G= MANE Select	NP_570901.3:p.Val372=