Canonical Allele Identifier: CA11098195

Gene: SLC11A1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218390700A>G , CM000664.2:g.218390700A>G	GRCh38
NC_000002.11:g.219255423A>G , CM000664.1:g.219255423A>G	GRCh37
NC_000002.10:g.218963667A>G	NCBI36
NG_012128.1:g.13672A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233202.11:c.955-498A>G MANE Select	ENSP00000233202.6:n.955-498A>G
ENST00000233202.10:c.955-498A>G	ENSP00000233202.6:n.955-498A>G
ENST00000354352.9:c.*537-498A>G	ENSP00000346320.5:n.*537-498A>G
ENST00000465984.5:n.1431-498A>G
ENST00000468221.5:n.3216-498A>G
ENST00000490872.1:n.65-498A>G
ENST00000494322.5:n.1051-498A>G
ENST00000539932.5:c.*563-498A>G	ENSP00000443435.2:n.*563-498A>G
NM_000578.3:c.955-498A>G	NP_000569.3:n.955-498A>G
XM_005246793.2:c.754-498A>G	XP_005246850.1:n.754-498A>G
XM_005246794.2:c.601-498A>G	XP_005246851.1:n.601-498A>G
XM_006712709.2:c.601-498A>G	XP_006712772.1:n.601-498A>G
XM_006712710.2:c.601-498A>G	XP_006712773.1:n.601-498A>G
XM_006712711.2:c.508-498A>G	XP_006712774.1:n.508-498A>G
XM_011511684.1:c.628-498A>G	XP_011509986.1:n.628-498A>G
XM_011511685.1:c.628-498A>G	XP_011509987.1:n.628-498A>G
XR_427107.1:n.1118-498A>G
XR_427108.2:n.1415-498A>G
XM_005246793.4:c.754-498A>G	XP_005246850.1:n.754-498A>G
XM_005246794.4:c.601-498A>G	XP_005246851.1:n.601-498A>G
XM_006712709.4:c.601-498A>G	XP_006712772.1:n.601-498A>G
XM_006712710.4:c.601-498A>G	XP_006712773.1:n.601-498A>G
XM_006712711.4:c.508-498A>G	XP_006712774.1:n.508-498A>G
XM_011511684.3:c.628-498A>G	XP_011509986.1:n.628-498A>G
XM_011511685.3:c.628-498A>G	XP_011509987.1:n.628-498A>G
XM_017004765.2:c.832-498A>G	XP_016860254.1:n.832-498A>G
XM_017004766.2:c.754-498A>G	XP_016860255.1:n.754-498A>G
XM_017004767.2:c.796-2281A>G	XP_016860256.1:n.796-2281A>G
XR_427107.3:n.1104-498A>G
XR_427108.4:n.1415-498A>G
NM_000578.4:c.955-498A>G MANE Select	NP_000569.3:n.955-498A>G