Canonical Allele Identifier: CA1328733605

Gene: SLC11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218384275C= , CM000664.2:g.218384275C=	GRCh38
NC_000002.11:g.219248998C= , CM000664.1:g.219248998C=	GRCh37
NC_000002.10:g.218957242C=	NCBI36
NG_012128.1:g.7247C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233202.11:c.183C= MANE Select	ENSP00000233202.6:p.Phe61=
ENST00000233202.10:c.183C=	ENSP00000233202.6:p.Phe61=
ENST00000354352.9:c.183C=	ENSP00000346320.5:p.Phe61=
ENST00000465984.5:n.332-872C=
ENST00000468221.5:n.1663C=
ENST00000469449.1:n.589C=
ENST00000469799.5:n.98-872C=
ENST00000471875.5:n.130C=
ENST00000473367.5:c.151-44C=	ENSP00000484905.1:n.151-44C=
ENST00000475225.5:n.186-44C=
ENST00000481524.5:c.8-872C=	ENSP00000483970.1:n.8-872C=
ENST00000483487.2:n.109C=
ENST00000492413.5:n.265C=
ENST00000494322.5:n.279C=
ENST00000539932.5:c.40C=	ENSP00000443435.2:p.His14=
NM_000578.3:c.183C=	NP_000569.3:p.Phe61=
XM_005246793.2:c.-19C=	XP_005246850.1:n.-19C=
XM_005246794.2:c.-246C=	XP_005246851.1:n.-246C=
XM_006712709.2:c.-246C=	XP_006712772.1:n.-246C=
XM_006712710.2:c.-155-872C=	XP_006712773.1:n.-155-872C=
XM_006712711.2:c.-174-872C=	XP_006712774.1:n.-174-872C=
XM_011511684.1:c.-254C=	XP_011509986.1:n.-254C=
XM_011511685.1:c.-254C=	XP_011509987.1:n.-254C=
XR_427107.1:n.346C=
XR_427108.2:n.643C=
XM_005246793.4:c.-19C=	XP_005246850.1:n.-19C=
XM_005246794.4:c.-246C=	XP_005246851.1:n.-246C=
XM_006712709.4:c.-246C=	XP_006712772.1:n.-246C=
XM_006712710.4:c.-155-872C=	XP_006712773.1:n.-155-872C=
XM_006712711.4:c.-174-872C=	XP_006712774.1:n.-174-872C=
XM_011511684.3:c.-254C=	XP_011509986.1:n.-254C=
XM_011511685.3:c.-254C=	XP_011509987.1:n.-254C=
XM_017004765.2:c.151-872C=	XP_016860254.1:n.151-872C=
XM_017004766.2:c.-19C=	XP_016860255.1:n.-19C=
XM_017004767.2:c.183C=	XP_016860256.1:p.Phe61=
XR_427107.3:n.332C=
XR_427108.4:n.643C=
NM_000578.4:c.183C= MANE Select	NP_000569.3:p.Phe61=