Canonical Allele Identifier: CA2663111957

Gene: SLC11A1

Linked Data

• gnomAD v4: 2-218384204-CCAGGACCCCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218384207_218384217del , CM000664.2:g.218384207_218384217del	GRCh38
NC_000002.11:g.219248930_219248940del , CM000664.1:g.219248930_219248940del	GRCh37
NC_000002.10:g.218957174_218957184del	NCBI36
NG_012128.1:g.7179_7189del

Transcript Alleles

HGVS	Amino-acid change
ENST00000233202.11:c.151-36_151-26del MANE Select	ENSP00000233202.6:n.151-36_151-26del
ENST00000233202.10:c.151-36_151-26del	ENSP00000233202.6:n.151-36_151-26del
ENST00000354352.9:c.151-36_151-26del	ENSP00000346320.5:n.151-36_151-26del
ENST00000465984.5:n.332-940_332-930del
ENST00000468221.5:n.1595_1605del
ENST00000469449.1:n.521_531del
ENST00000469799.5:n.98-940_98-930del
ENST00000471875.5:n.98-36_98-26del
ENST00000473367.5:c.151-112_151-102del	ENSP00000484905.1:n.151-112_151-102del
ENST00000475225.5:n.186-112_186-102del
ENST00000481524.5:c.8-940_8-930del	ENSP00000483970.1:n.8-940_8-930del
ENST00000483487.2:n.41_51del
ENST00000492413.5:n.233-36_233-26del
ENST00000494322.5:n.247-36_247-26del
ENST00000539932.5:c.8-36_8-26del	ENSP00000443435.2:n.8-36_8-26del
NM_000578.3:c.151-36_151-26del	NP_000569.3:n.151-36_151-26del
XM_005246793.2:c.-51-36_-51-26del	XP_005246850.1:n.-51-36_-51-26del
XM_005246794.2:c.-278-36_-278-26del	XP_005246851.1:n.-278-36_-278-26del
XM_006712709.2:c.-278-36_-278-26del	XP_006712772.1:n.-278-36_-278-26del
XM_006712710.2:c.-155-940_-155-930del	XP_006712773.1:n.-155-940_-155-930del
XM_006712711.2:c.-174-940_-174-930del	XP_006712774.1:n.-174-940_-174-930del
XM_011511684.1:c.-286-36_-286-26del	XP_011509986.1:n.-286-36_-286-26del
XM_011511685.1:c.-286-36_-286-26del	XP_011509987.1:n.-286-36_-286-26del
XR_427107.1:n.314-36_314-26del
XR_427108.2:n.611-36_611-26del
XM_005246793.4:c.-51-36_-51-26del	XP_005246850.1:n.-51-36_-51-26del
XM_005246794.4:c.-278-36_-278-26del	XP_005246851.1:n.-278-36_-278-26del
XM_006712709.4:c.-278-36_-278-26del	XP_006712772.1:n.-278-36_-278-26del
XM_006712710.4:c.-155-940_-155-930del	XP_006712773.1:n.-155-940_-155-930del
XM_006712711.4:c.-174-940_-174-930del	XP_006712774.1:n.-174-940_-174-930del
XM_011511684.3:c.-286-36_-286-26del	XP_011509986.1:n.-286-36_-286-26del
XM_011511685.3:c.-286-36_-286-26del	XP_011509987.1:n.-286-36_-286-26del
XM_017004765.2:c.151-940_151-930del	XP_016860254.1:n.151-940_151-930del
XM_017004766.2:c.-51-36_-51-26del	XP_016860255.1:n.-51-36_-51-26del
XM_017004767.2:c.151-36_151-26del	XP_016860256.1:n.151-36_151-26del
XR_427107.3:n.300-36_300-26del
XR_427108.4:n.611-36_611-26del
NM_000578.4:c.151-36_151-26del MANE Select	NP_000569.3:n.151-36_151-26del