Canonical Allele Identifier: CA2346474922
Gene: SLC4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3228288G= , CM000682.2:g.3228288G= GRCh38
NC_000020.10:g.3208934G= , CM000682.1:g.3208934G= GRCh37
NC_000020.9:g.3156934G= NCBI36
NG_017072.1:g.15954C=
NG_012093.2:g.24422G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642402.1:c.2529C= MANE Select ENSP00000493503.1:p.Pro843=
ENST00000644011.1:c.2460C= ENSP00000496214.1:p.Pro820=
ENST00000644692.1:c.2328C= ENSP00000493824.1:p.Pro776=
ENST00000647296.1:c.2415C= ENSP00000495050.1:p.Pro805=
ENST00000380056.7:c.2577C= ENSP00000369396.3:p.Pro859=
ENST00000380059.7:c.2658C= ENSP00000369399.3:p.Pro886=
ENST00000474451.5:c.*677C= ENSP00000476859.1:n.*677C=
ENST00000539553.6:c.2529C= ENSP00000441370.1:p.Pro843=
NM_001174089.1:c.2529C= NP_001167560.1:p.Pro843=
NM_001174090.1:c.2658C= NP_001167561.1:p.Pro886=
NM_032034.3:c.2577C= NP_114423.1:p.Pro859=
XM_005260856.3:c.2898C= XP_005260913.1:p.Pro966=
XM_005260857.1:c.2472C= XP_005260914.1:p.Pro824=
XM_011529383.1:c.2496C= XP_011527685.1:p.Pro832=
XM_011529384.1:c.2472C= XP_011527686.1:p.Pro824=
XM_011529385.1:c.2472C= XP_011527687.1:p.Pro824=
XR_937167.1:n.2627C=
NM_001363745.1:c.2415C= NP_001350674.1:p.Pro805=
NR_135000.1:n.2627C=
XM_005260856.5:c.2898C= XP_005260913.1:p.Pro966=
XM_011529383.3:c.2496C= XP_011527685.1:p.Pro832=
XM_017028093.1:c.2892C= XP_016883582.1:p.Pro964=
XM_017028094.1:c.2472C= XP_016883583.1:p.Pro824=
XM_017028096.1:c.2472C= XP_016883585.1:p.Pro824=
XR_001754419.1:n.3072C=
XR_001754420.2:n.3052C=
NM_001174089.2:c.2529C= MANE Select NP_001167560.1:p.Pro843=
NM_001363745.2:c.2415C= NP_001350674.1:p.Pro805=
NM_001174090.2:c.2658C= NP_001167561.1:p.Pro886=
NM_032034.4:c.2577C= NP_114423.1:p.Pro859=
NM_001400277.1:c.2472C= NP_001387206.1:p.Pro824=
NM_001400278.1:c.2472C= NP_001387207.1:p.Pro824=
NM_001400279.1:c.2472C= NP_001387208.1:p.Pro824=
NM_001400280.1:c.2544C= NP_001387209.1:p.Pro848=
NR_174470.1:n.3052C=
NR_174471.1:n.3037C=