Canonical Allele Identifier: CA1328733563

Gene: SLC11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218384216C= , CM000664.2:g.218384216C=	GRCh38
NC_000002.11:g.219248939C= , CM000664.1:g.219248939C=	GRCh37
NC_000002.10:g.218957183C=	NCBI36
NG_012128.1:g.7188C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000233202.11:c.151-27C= MANE Select	ENSP00000233202.6:n.151-27C=
ENST00000233202.10:c.151-27C=	ENSP00000233202.6:n.151-27C=
ENST00000354352.9:c.151-27C=	ENSP00000346320.5:n.151-27C=
ENST00000465984.5:n.332-931C=
ENST00000468221.5:n.1604C=
ENST00000469449.1:n.530C=
ENST00000469799.5:n.98-931C=
ENST00000471875.5:n.98-27C=
ENST00000473367.5:c.151-103C=	ENSP00000484905.1:n.151-103C=
ENST00000475225.5:n.186-103C=
ENST00000481524.5:c.8-931C=	ENSP00000483970.1:n.8-931C=
ENST00000483487.2:n.50C=
ENST00000492413.5:n.233-27C=
ENST00000494322.5:n.247-27C=
ENST00000539932.5:c.8-27C=	ENSP00000443435.2:n.8-27C=
NM_000578.3:c.151-27C=	NP_000569.3:n.151-27C=
XM_005246793.2:c.-51-27C=	XP_005246850.1:n.-51-27C=
XM_005246794.2:c.-278-27C=	XP_005246851.1:n.-278-27C=
XM_006712709.2:c.-278-27C=	XP_006712772.1:n.-278-27C=
XM_006712710.2:c.-155-931C=	XP_006712773.1:n.-155-931C=
XM_006712711.2:c.-174-931C=	XP_006712774.1:n.-174-931C=
XM_011511684.1:c.-286-27C=	XP_011509986.1:n.-286-27C=
XM_011511685.1:c.-286-27C=	XP_011509987.1:n.-286-27C=
XR_427107.1:n.314-27C=
XR_427108.2:n.611-27C=
XM_005246793.4:c.-51-27C=	XP_005246850.1:n.-51-27C=
XM_005246794.4:c.-278-27C=	XP_005246851.1:n.-278-27C=
XM_006712709.4:c.-278-27C=	XP_006712772.1:n.-278-27C=
XM_006712710.4:c.-155-931C=	XP_006712773.1:n.-155-931C=
XM_006712711.4:c.-174-931C=	XP_006712774.1:n.-174-931C=
XM_011511684.3:c.-286-27C=	XP_011509986.1:n.-286-27C=
XM_011511685.3:c.-286-27C=	XP_011509987.1:n.-286-27C=
XM_017004765.2:c.151-931C=	XP_016860254.1:n.151-931C=
XM_017004766.2:c.-51-27C=	XP_016860255.1:n.-51-27C=
XM_017004767.2:c.151-27C=	XP_016860256.1:n.151-27C=
XR_427107.3:n.300-27C=
XR_427108.4:n.611-27C=
NM_000578.4:c.151-27C= MANE Select	NP_000569.3:n.151-27C=