Canonical Allele Identifier: CA350541831

Gene: SLC11A1

Linked Data

• MyVariant Identifiers: chr2:g.219249014C>G (hg19) ; chr2:g.218384291C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218384291C>G , CM000664.2:g.218384291C>G	GRCh38
NC_000002.11:g.219249014C>G , CM000664.1:g.219249014C>G	GRCh37
NC_000002.10:g.218957258C>G	NCBI36
NG_012128.1:g.7263C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233202.11:c.199C>G MANE Select	ENSP00000233202.6:p.Leu67Val
ENST00000233202.10:c.199C>G	ENSP00000233202.6:p.Leu67Val
ENST00000354352.9:c.199C>G	ENSP00000346320.5:p.Leu67Val
ENST00000465984.5:n.332-856C>G
ENST00000468221.5:n.1679C>G
ENST00000469449.1:n.605C>G
ENST00000469799.5:n.98-856C>G
ENST00000471875.5:n.146C>G
ENST00000473367.5:c.151-28C>G	ENSP00000484905.1:n.151-28C>G
ENST00000475225.5:n.186-28C>G
ENST00000481524.5:c.8-856C>G	ENSP00000483970.1:n.8-856C>G
ENST00000483487.2:n.125C>G
ENST00000492413.5:n.281C>G
ENST00000494322.5:n.295C>G
ENST00000539932.5:c.56C>G	ENSP00000443435.2:p.Pro19Arg
NM_000578.3:c.199C>G	NP_000569.3:p.Leu67Val
XM_005246793.2:c.-3C>G	XP_005246850.1:n.-3C>G
XM_005246794.2:c.-230C>G	XP_005246851.1:n.-230C>G
XM_006712709.2:c.-230C>G	XP_006712772.1:n.-230C>G
XM_006712710.2:c.-155-856C>G	XP_006712773.1:n.-155-856C>G
XM_006712711.2:c.-174-856C>G	XP_006712774.1:n.-174-856C>G
XM_011511684.1:c.-238C>G	XP_011509986.1:n.-238C>G
XM_011511685.1:c.-238C>G	XP_011509987.1:n.-238C>G
XR_427107.1:n.362C>G
XR_427108.2:n.659C>G
XM_005246793.4:c.-3C>G	XP_005246850.1:n.-3C>G
XM_005246794.4:c.-230C>G	XP_005246851.1:n.-230C>G
XM_006712709.4:c.-230C>G	XP_006712772.1:n.-230C>G
XM_006712710.4:c.-155-856C>G	XP_006712773.1:n.-155-856C>G
XM_006712711.4:c.-174-856C>G	XP_006712774.1:n.-174-856C>G
XM_011511684.3:c.-238C>G	XP_011509986.1:n.-238C>G
XM_011511685.3:c.-238C>G	XP_011509987.1:n.-238C>G
XM_017004765.2:c.151-856C>G	XP_016860254.1:n.151-856C>G
XM_017004766.2:c.-3C>G	XP_016860255.1:n.-3C>G
XM_017004767.2:c.199C>G	XP_016860256.1:p.Leu67Val
XR_427107.3:n.348C>G
XR_427108.4:n.659C>G
NM_000578.4:c.199C>G MANE Select	NP_000569.3:p.Leu67Val