Canonical Allele Identifier: CA4941552

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144415027G= , CM000670.2:g.144415027G=	GRCh38
NG_012234.2:g.6864C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.751C= MANE Select	ENSP00000301305.4:p.Arg251=
ENST00000276833.9:c.676C=	ENSP00000276833.5:p.Arg226=
ENST00000301305.7:c.751C=	ENSP00000301305.3:p.Arg251=
ENST00000526658.1:c.469C=	ENSP00000434512.1:p.Arg157=
NM_017767.2:c.676C=	NP_060237.2:p.Arg226=
NM_130849.3:c.751C=	NP_570901.2:p.Arg251=
XM_006716599.1:c.751C=	XP_006716662.1:p.Arg251=
XM_011517153.1:c.469C=	XP_011515455.1:p.Arg157=
XM_024447188.1:c.469C=	XP_024302956.1:p.Arg157=
XM_024447189.1:c.469C=	XP_024302957.1:p.Arg157=
NM_001374839.1:c.469C=	NP_001361768.1:p.Arg157=
NM_017767.3:c.676C=	NP_060237.3:p.Arg226=
NM_130849.4:c.751C= MANE Select	NP_570901.3:p.Arg251=