Canonical Allele Identifier: CA431217624

Gene: SLC11A1

Linked Data

• MyVariant Identifiers: chr2:g.219249046C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218384323C>T , CM000664.2:g.218384323C>T	GRCh38
NC_000002.11:g.219249046C>T , CM000664.1:g.219249046C>T	GRCh37
NC_000002.10:g.218957290C>T	NCBI36
NG_012128.1:g.7295C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233202.11:c.231C>T MANE Select	ENSP00000233202.6:p.Asn77=
ENST00000233202.10:c.231C>T	ENSP00000233202.6:p.Asn77=
ENST00000354352.9:c.231C>T	ENSP00000346320.5:p.Asn77=
ENST00000465984.5:n.332-824C>T
ENST00000468221.5:n.1711C>T
ENST00000469449.1:n.637C>T
ENST00000469799.5:n.98-824C>T
ENST00000471875.5:n.178C>T
ENST00000473367.5:c.155C>T	ENSP00000484905.1:p.Thr52Ile
ENST00000475225.5:n.190C>T
ENST00000481524.5:c.8-824C>T	ENSP00000483970.1:n.8-824C>T
ENST00000483487.2:n.157C>T
ENST00000492413.5:n.313C>T
ENST00000494322.5:n.327C>T
ENST00000539932.5:c.88C>T	ENSP00000443435.2:p.His30Tyr
NM_000578.3:c.231C>T	NP_000569.3:p.Asn77=
XM_005246793.2:c.30C>T	XP_005246850.1:p.Asn10=
XM_005246794.2:c.-198C>T	XP_005246851.1:n.-198C>T
XM_006712709.2:c.-198C>T	XP_006712772.1:n.-198C>T
XM_006712710.2:c.-155-824C>T	XP_006712773.1:n.-155-824C>T
XM_006712711.2:c.-174-824C>T	XP_006712774.1:n.-174-824C>T
XM_011511684.1:c.-206C>T	XP_011509986.1:n.-206C>T
XM_011511685.1:c.-206C>T	XP_011509987.1:n.-206C>T
XR_427107.1:n.394C>T
XR_427108.2:n.691C>T
XM_005246793.4:c.30C>T	XP_005246850.1:p.Asn10=
XM_005246794.4:c.-198C>T	XP_005246851.1:n.-198C>T
XM_006712709.4:c.-198C>T	XP_006712772.1:n.-198C>T
XM_006712710.4:c.-155-824C>T	XP_006712773.1:n.-155-824C>T
XM_006712711.4:c.-174-824C>T	XP_006712774.1:n.-174-824C>T
XM_011511684.3:c.-206C>T	XP_011509986.1:n.-206C>T
XM_011511685.3:c.-206C>T	XP_011509987.1:n.-206C>T
XM_017004765.2:c.151-824C>T	XP_016860254.1:n.151-824C>T
XM_017004766.2:c.30C>T	XP_016860255.1:p.Asn10=
XM_017004767.2:c.231C>T	XP_016860256.1:p.Asn77=
XR_427107.3:n.380C>T
XR_427108.4:n.691C>T
NM_000578.4:c.231C>T MANE Select	NP_000569.3:p.Asn77=