Canonical Allele Identifier: CA1328733595

Gene: SLC11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218384257G= , CM000664.2:g.218384257G=	GRCh38
NC_000002.11:g.219248980G= , CM000664.1:g.219248980G=	GRCh37
NC_000002.10:g.218957224G=	NCBI36
NG_012128.1:g.7229G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233202.11:c.165G= MANE Select	ENSP00000233202.6:p.Leu55=
ENST00000233202.10:c.165G=	ENSP00000233202.6:p.Leu55=
ENST00000354352.9:c.165G=	ENSP00000346320.5:p.Leu55=
ENST00000465984.5:n.332-890G=
ENST00000468221.5:n.1645G=
ENST00000469449.1:n.571G=
ENST00000469799.5:n.98-890G=
ENST00000471875.5:n.112G=
ENST00000473367.5:c.151-62G=	ENSP00000484905.1:n.151-62G=
ENST00000475225.5:n.186-62G=
ENST00000481524.5:c.8-890G=	ENSP00000483970.1:n.8-890G=
ENST00000483487.2:n.91G=
ENST00000492413.5:n.247G=
ENST00000494322.5:n.261G=
ENST00000539932.5:c.22G=	ENSP00000443435.2:p.Ala8=
NM_000578.3:c.165G=	NP_000569.3:p.Leu55=
XM_005246793.2:c.-37G=	XP_005246850.1:n.-37G=
XM_005246794.2:c.-264G=	XP_005246851.1:n.-264G=
XM_006712709.2:c.-264G=	XP_006712772.1:n.-264G=
XM_006712710.2:c.-155-890G=	XP_006712773.1:n.-155-890G=
XM_006712711.2:c.-174-890G=	XP_006712774.1:n.-174-890G=
XM_011511684.1:c.-272G=	XP_011509986.1:n.-272G=
XM_011511685.1:c.-272G=	XP_011509987.1:n.-272G=
XR_427107.1:n.328G=
XR_427108.2:n.625G=
XM_005246793.4:c.-37G=	XP_005246850.1:n.-37G=
XM_005246794.4:c.-264G=	XP_005246851.1:n.-264G=
XM_006712709.4:c.-264G=	XP_006712772.1:n.-264G=
XM_006712710.4:c.-155-890G=	XP_006712773.1:n.-155-890G=
XM_006712711.4:c.-174-890G=	XP_006712774.1:n.-174-890G=
XM_011511684.3:c.-272G=	XP_011509986.1:n.-272G=
XM_011511685.3:c.-272G=	XP_011509987.1:n.-272G=
XM_017004765.2:c.151-890G=	XP_016860254.1:n.151-890G=
XM_017004766.2:c.-37G=	XP_016860255.1:n.-37G=
XM_017004767.2:c.165G=	XP_016860256.1:p.Leu55=
XR_427107.3:n.314G=
XR_427108.4:n.625G=
NM_000578.4:c.165G= MANE Select	NP_000569.3:p.Leu55=