Canonical Allele Identifier: CA2839530462

Gene: SLC11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218384181G>C , CM000664.2:g.218384181G>C	GRCh38
NC_000002.11:g.219248904G>C , CM000664.1:g.219248904G>C	GRCh37
NC_000002.10:g.218957148G>C	NCBI36
NG_012128.1:g.7153G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233202.11:c.151-62G>C MANE Select	ENSP00000233202.6:n.151-62G>C
ENST00000233202.10:c.151-62G>C	ENSP00000233202.6:n.151-62G>C
ENST00000354352.9:c.151-62G>C	ENSP00000346320.5:n.151-62G>C
ENST00000465984.5:n.332-966G>C
ENST00000468221.5:n.1569G>C
ENST00000469449.1:n.495G>C
ENST00000469799.5:n.98-966G>C
ENST00000471875.5:n.98-62G>C
ENST00000473367.5:c.151-138G>C	ENSP00000484905.1:n.151-138G>C
ENST00000475225.5:n.186-138G>C
ENST00000481524.5:c.8-966G>C	ENSP00000483970.1:n.8-966G>C
ENST00000483487.2:n.15G>C
ENST00000492413.5:n.233-62G>C
ENST00000494322.5:n.247-62G>C
ENST00000539932.5:c.8-62G>C	ENSP00000443435.2:n.8-62G>C
NM_000578.3:c.151-62G>C	NP_000569.3:n.151-62G>C
XM_005246793.2:c.-51-62G>C	XP_005246850.1:n.-51-62G>C
XM_005246794.2:c.-278-62G>C	XP_005246851.1:n.-278-62G>C
XM_006712709.2:c.-278-62G>C	XP_006712772.1:n.-278-62G>C
XM_006712710.2:c.-155-966G>C	XP_006712773.1:n.-155-966G>C
XM_006712711.2:c.-174-966G>C	XP_006712774.1:n.-174-966G>C
XM_011511684.1:c.-286-62G>C	XP_011509986.1:n.-286-62G>C
XM_011511685.1:c.-286-62G>C	XP_011509987.1:n.-286-62G>C
XR_427107.1:n.314-62G>C
XR_427108.2:n.611-62G>C
XM_005246793.4:c.-51-62G>C	XP_005246850.1:n.-51-62G>C
XM_005246794.4:c.-278-62G>C	XP_005246851.1:n.-278-62G>C
XM_006712709.4:c.-278-62G>C	XP_006712772.1:n.-278-62G>C
XM_006712710.4:c.-155-966G>C	XP_006712773.1:n.-155-966G>C
XM_006712711.4:c.-174-966G>C	XP_006712774.1:n.-174-966G>C
XM_011511684.3:c.-286-62G>C	XP_011509986.1:n.-286-62G>C
XM_011511685.3:c.-286-62G>C	XP_011509987.1:n.-286-62G>C
XM_017004765.2:c.151-966G>C	XP_016860254.1:n.151-966G>C
XM_017004766.2:c.-51-62G>C	XP_016860255.1:n.-51-62G>C
XM_017004767.2:c.151-62G>C	XP_016860256.1:n.151-62G>C
XR_427107.3:n.300-62G>C
XR_427108.4:n.611-62G>C
NM_000578.4:c.151-62G>C MANE Select	NP_000569.3:n.151-62G>C