Canonical Allele Identifier: CA764880018

Gene: SLC11A1

Linked Data

• dbSNP Id: rs1431491084
• gnomAD v4: 2-218384204-C-G
• MyVariant Identifiers: chr2:g.219248927C>G (hg19) ; chr2:g.218384204C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218384204C>G , CM000664.2:g.218384204C>G	GRCh38
NC_000002.11:g.219248927C>G , CM000664.1:g.219248927C>G	GRCh37
NC_000002.10:g.218957171C>G	NCBI36
NG_012128.1:g.7176C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000233202.11:c.151-39C>G MANE Select	ENSP00000233202.6:n.151-39C>G
ENST00000233202.10:c.151-39C>G	ENSP00000233202.6:n.151-39C>G
ENST00000354352.9:c.151-39C>G	ENSP00000346320.5:n.151-39C>G
ENST00000465984.5:n.332-943C>G
ENST00000468221.5:n.1592C>G
ENST00000469449.1:n.518C>G
ENST00000469799.5:n.98-943C>G
ENST00000471875.5:n.98-39C>G
ENST00000473367.5:c.151-115C>G	ENSP00000484905.1:n.151-115C>G
ENST00000475225.5:n.186-115C>G
ENST00000481524.5:c.8-943C>G	ENSP00000483970.1:n.8-943C>G
ENST00000483487.2:n.38C>G
ENST00000492413.5:n.233-39C>G
ENST00000494322.5:n.247-39C>G
ENST00000539932.5:c.8-39C>G	ENSP00000443435.2:n.8-39C>G
NM_000578.3:c.151-39C>G	NP_000569.3:n.151-39C>G
XM_005246793.2:c.-51-39C>G	XP_005246850.1:n.-51-39C>G
XM_005246794.2:c.-278-39C>G	XP_005246851.1:n.-278-39C>G
XM_006712709.2:c.-278-39C>G	XP_006712772.1:n.-278-39C>G
XM_006712710.2:c.-155-943C>G	XP_006712773.1:n.-155-943C>G
XM_006712711.2:c.-174-943C>G	XP_006712774.1:n.-174-943C>G
XM_011511684.1:c.-286-39C>G	XP_011509986.1:n.-286-39C>G
XM_011511685.1:c.-286-39C>G	XP_011509987.1:n.-286-39C>G
XR_427107.1:n.314-39C>G
XR_427108.2:n.611-39C>G
XM_005246793.4:c.-51-39C>G	XP_005246850.1:n.-51-39C>G
XM_005246794.4:c.-278-39C>G	XP_005246851.1:n.-278-39C>G
XM_006712709.4:c.-278-39C>G	XP_006712772.1:n.-278-39C>G
XM_006712710.4:c.-155-943C>G	XP_006712773.1:n.-155-943C>G
XM_006712711.4:c.-174-943C>G	XP_006712774.1:n.-174-943C>G
XM_011511684.3:c.-286-39C>G	XP_011509986.1:n.-286-39C>G
XM_011511685.3:c.-286-39C>G	XP_011509987.1:n.-286-39C>G
XM_017004765.2:c.151-943C>G	XP_016860254.1:n.151-943C>G
XM_017004766.2:c.-51-39C>G	XP_016860255.1:n.-51-39C>G
XM_017004767.2:c.151-39C>G	XP_016860256.1:n.151-39C>G
XR_427107.3:n.300-39C>G
XR_427108.4:n.611-39C>G
NM_000578.4:c.151-39C>G MANE Select	NP_000569.3:n.151-39C>G