Canonical Allele Identifier: CA1328738732

Gene: SLC11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218394939C= , CM000664.2:g.218394939C=	GRCh38
NC_000002.11:g.219259662C= , CM000664.1:g.219259662C=	GRCh37
NC_000002.10:g.218967906C=	NCBI36
NG_012128.1:g.17911C=
NG_030418.1:g.1602C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233202.11:c.1557C= MANE Select	ENSP00000233202.6:p.Cys519=
ENST00000233202.10:c.1557C=	ENSP00000233202.6:p.Cys519=
ENST00000354352.9:c.*1139C=	ENSP00000346320.5:n.*1139C=
ENST00000465984.5:n.2033C=
ENST00000468221.5:n.4684C=
NM_000578.3:c.1557C=	NP_000569.3:p.Cys519=
XM_005246793.2:c.1356C=	XP_005246850.1:p.Cys452=
XM_005246794.2:c.1203C=	XP_005246851.1:p.Cys401=
XM_006712709.2:c.1203C=	XP_006712772.1:p.Cys401=
XM_006712710.2:c.1203C=	XP_006712773.1:p.Cys401=
XM_006712711.2:c.1110C=	XP_006712774.1:p.Cys370=
XM_011511684.1:c.1230C=	XP_011509986.1:p.Cys410=
XM_011511685.1:c.1230C=	XP_011509987.1:p.Cys410=
XM_005246793.4:c.1356C=	XP_005246850.1:p.Cys452=
XM_005246794.4:c.1203C=	XP_005246851.1:p.Cys401=
XM_006712709.4:c.1203C=	XP_006712772.1:p.Cys401=
XM_006712710.4:c.1203C=	XP_006712773.1:p.Cys401=
XM_006712711.4:c.1110C=	XP_006712774.1:p.Cys370=
XM_011511684.3:c.1230C=	XP_011509986.1:p.Cys410=
XM_011511685.3:c.1230C=	XP_011509987.1:p.Cys410=
XM_017004765.2:c.1434C=	XP_016860254.1:p.Cys478=
XM_017004766.2:c.1356C=	XP_016860255.1:p.Cys452=
XM_017004767.2:c.1188C=	XP_016860256.1:p.Cys396=
XR_427107.3:n.2572C=
XR_427108.4:n.2883C=
NM_000578.4:c.1557C= MANE Select	NP_000569.3:p.Cys519=