Canonical Allele Identifier: CA1328738728

Gene: SLC11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218394932C= , CM000664.2:g.218394932C=	GRCh38
NC_000002.11:g.219259655C= , CM000664.1:g.219259655C=	GRCh37
NC_000002.10:g.218967899C=	NCBI36
NG_012128.1:g.17904C=
NG_030418.1:g.1595C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233202.11:c.1550C= MANE Select	ENSP00000233202.6:p.Thr517=
ENST00000233202.10:c.1550C=	ENSP00000233202.6:p.Thr517=
ENST00000354352.9:c.*1132C=	ENSP00000346320.5:n.*1132C=
ENST00000465984.5:n.2026C=
ENST00000468221.5:n.4677C=
NM_000578.3:c.1550C=	NP_000569.3:p.Thr517=
XM_005246793.2:c.1349C=	XP_005246850.1:p.Thr450=
XM_005246794.2:c.1196C=	XP_005246851.1:p.Thr399=
XM_006712709.2:c.1196C=	XP_006712772.1:p.Thr399=
XM_006712710.2:c.1196C=	XP_006712773.1:p.Thr399=
XM_006712711.2:c.1103C=	XP_006712774.1:p.Thr368=
XM_011511684.1:c.1223C=	XP_011509986.1:p.Thr408=
XM_011511685.1:c.1223C=	XP_011509987.1:p.Thr408=
XM_005246793.4:c.1349C=	XP_005246850.1:p.Thr450=
XM_005246794.4:c.1196C=	XP_005246851.1:p.Thr399=
XM_006712709.4:c.1196C=	XP_006712772.1:p.Thr399=
XM_006712710.4:c.1196C=	XP_006712773.1:p.Thr399=
XM_006712711.4:c.1103C=	XP_006712774.1:p.Thr368=
XM_011511684.3:c.1223C=	XP_011509986.1:p.Thr408=
XM_011511685.3:c.1223C=	XP_011509987.1:p.Thr408=
XM_017004765.2:c.1427C=	XP_016860254.1:p.Thr476=
XM_017004766.2:c.1349C=	XP_016860255.1:p.Thr450=
XM_017004767.2:c.1181C=	XP_016860256.1:p.Thr394=
XR_427107.3:n.2565C=
XR_427108.4:n.2876C=
NM_000578.4:c.1550C= MANE Select	NP_000569.3:p.Thr517=