Canonical Allele Identifier: CA2701543268

Gene: SLC11A1

Linked Data

• dbSNP Id: rs2106328319

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218384206_218384225dup , CM000664.2:g.218384206_218384225dup	GRCh38
NC_000002.11:g.219248929_219248948dup , CM000664.1:g.219248929_219248948dup	GRCh37
NC_000002.10:g.218957173_218957192dup	NCBI36
NG_012128.1:g.7178_7197dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000233202.11:c.151-37_151-18dup MANE Select	ENSP00000233202.6:n.151-37_151-18dup
ENST00000233202.10:c.151-37_151-18dup	ENSP00000233202.6:n.151-37_151-18dup
ENST00000354352.9:c.151-37_151-18dup	ENSP00000346320.5:n.151-37_151-18dup
ENST00000465984.5:n.332-941_332-922dup
ENST00000468221.5:n.1594_1613dup
ENST00000469449.1:n.520_539dup
ENST00000469799.5:n.98-941_98-922dup
ENST00000471875.5:n.98-37_98-18dup
ENST00000473367.5:c.151-113_151-94dup	ENSP00000484905.1:n.151-113_151-94dup
ENST00000475225.5:n.186-113_186-94dup
ENST00000481524.5:c.8-941_8-922dup	ENSP00000483970.1:n.8-941_8-922dup
ENST00000483487.2:n.40_59dup
ENST00000492413.5:n.233-37_233-18dup
ENST00000494322.5:n.247-37_247-18dup
ENST00000539932.5:c.8-37_8-18dup	ENSP00000443435.2:n.8-37_8-18dup
NM_000578.3:c.151-37_151-18dup	NP_000569.3:n.151-37_151-18dup
XM_005246793.2:c.-51-37_-51-18dup	XP_005246850.1:n.-51-37_-51-18dup
XM_005246794.2:c.-278-37_-278-18dup	XP_005246851.1:n.-278-37_-278-18dup
XM_006712709.2:c.-278-37_-278-18dup	XP_006712772.1:n.-278-37_-278-18dup
XM_006712710.2:c.-155-941_-155-922dup	XP_006712773.1:n.-155-941_-155-922dup
XM_006712711.2:c.-174-941_-174-922dup	XP_006712774.1:n.-174-941_-174-922dup
XM_011511684.1:c.-286-37_-286-18dup	XP_011509986.1:n.-286-37_-286-18dup
XM_011511685.1:c.-286-37_-286-18dup	XP_011509987.1:n.-286-37_-286-18dup
XR_427107.1:n.314-37_314-18dup
XR_427108.2:n.611-37_611-18dup
XM_005246793.4:c.-51-37_-51-18dup	XP_005246850.1:n.-51-37_-51-18dup
XM_005246794.4:c.-278-37_-278-18dup	XP_005246851.1:n.-278-37_-278-18dup
XM_006712709.4:c.-278-37_-278-18dup	XP_006712772.1:n.-278-37_-278-18dup
XM_006712710.4:c.-155-941_-155-922dup	XP_006712773.1:n.-155-941_-155-922dup
XM_006712711.4:c.-174-941_-174-922dup	XP_006712774.1:n.-174-941_-174-922dup
XM_011511684.3:c.-286-37_-286-18dup	XP_011509986.1:n.-286-37_-286-18dup
XM_011511685.3:c.-286-37_-286-18dup	XP_011509987.1:n.-286-37_-286-18dup
XM_017004765.2:c.151-941_151-922dup	XP_016860254.1:n.151-941_151-922dup
XM_017004766.2:c.-51-37_-51-18dup	XP_016860255.1:n.-51-37_-51-18dup
XM_017004767.2:c.151-37_151-18dup	XP_016860256.1:n.151-37_151-18dup
XR_427107.3:n.300-37_300-18dup
XR_427108.4:n.611-37_611-18dup
NM_000578.4:c.151-37_151-18dup MANE Select	NP_000569.3:n.151-37_151-18dup