Canonical Allele Identifier: CA1042458385

Gene: SLC11A1

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218387485C>G , CM000664.2:g.218387485C>G	GRCh38
NC_000002.11:g.219252208C>G , CM000664.1:g.219252208C>G	GRCh37
NC_000002.10:g.218960452C>G	NCBI36
NG_012128.1:g.10457C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233202.11:c.572-80C>G MANE Select	ENSP00000233202.6:n.572-80C>G
ENST00000233202.10:c.572-80C>G	ENSP00000233202.6:n.572-80C>G
ENST00000354352.9:c.*154-80C>G	ENSP00000346320.5:n.*154-80C>G
ENST00000465984.5:n.1048-80C>G
ENST00000468221.5:n.2833-80C>G
ENST00000469449.1:n.1615-80C>G
ENST00000475225.5:n.949-80C>G
ENST00000481524.5:c.*180-80C>G	ENSP00000483970.1:n.*180-80C>G
ENST00000494322.5:n.668-80C>G
ENST00000539932.5:c.*180-80C>G	ENSP00000443435.2:n.*180-80C>G
NM_000578.3:c.572-80C>G	NP_000569.3:n.572-80C>G
XM_005246793.2:c.371-80C>G	XP_005246850.1:n.371-80C>G
XM_005246794.2:c.218-80C>G	XP_005246851.1:n.218-80C>G
XM_006712709.2:c.218-80C>G	XP_006712772.1:n.218-80C>G
XM_006712710.2:c.218-80C>G	XP_006712773.1:n.218-80C>G
XM_006712711.2:c.125-80C>G	XP_006712774.1:n.125-80C>G
XM_011511684.1:c.245-80C>G	XP_011509986.1:n.245-80C>G
XM_011511685.1:c.245-80C>G	XP_011509987.1:n.245-80C>G
XR_427107.1:n.735-80C>G
XR_427108.2:n.1032-80C>G
XM_005246793.4:c.371-80C>G	XP_005246850.1:n.371-80C>G
XM_005246794.4:c.218-80C>G	XP_005246851.1:n.218-80C>G
XM_006712709.4:c.218-80C>G	XP_006712772.1:n.218-80C>G
XM_006712710.4:c.218-80C>G	XP_006712773.1:n.218-80C>G
XM_006712711.4:c.125-80C>G	XP_006712774.1:n.125-80C>G
XM_011511684.3:c.245-80C>G	XP_011509986.1:n.245-80C>G
XM_011511685.3:c.245-80C>G	XP_011509987.1:n.245-80C>G
XM_017004765.2:c.449-80C>G	XP_016860254.1:n.449-80C>G
XM_017004766.2:c.371-80C>G	XP_016860255.1:n.371-80C>G
XM_017004767.2:c.572-80C>G	XP_016860256.1:n.572-80C>G
XR_427107.3:n.721-80C>G
XR_427108.4:n.1032-80C>G
NM_000578.4:c.572-80C>G MANE Select	NP_000569.3:n.572-80C>G