Canonical Allele Identifier: CA2651690987
Gene: SLC4A11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3228135_3228136insTG , CM000682.2:g.3228135_3228136insTG GRCh38
NC_000020.10:g.3208781_3208782insTG , CM000682.1:g.3208781_3208782insTG GRCh37
NC_000020.9:g.3156781_3156782insTG NCBI36
NG_017072.1:g.16106_16107insCA
NG_012093.2:g.24269_24270insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000642402.1:c.2558+123_2558+124insCA MANE Select ENSP00000493503.1:n.2558+123_2558+124insCA
ENST00000644011.1:c.2489+123_2489+124insCA ENSP00000496214.1:n.2489+123_2489+124insCA
ENST00000644692.1:c.2357+123_2357+124insCA ENSP00000493824.1:n.2357+123_2357+124insCA
ENST00000647296.1:c.2444+123_2444+124insCA ENSP00000495050.1:n.2444+123_2444+124insCA
ENST00000380056.7:c.2606+123_2606+124insCA ENSP00000369396.3:n.2606+123_2606+124insCA
ENST00000380059.7:c.2687+123_2687+124insCA ENSP00000369399.3:n.2687+123_2687+124insCA
ENST00000474451.5:c.*706+123_*706+124insCA ENSP00000476859.1:n.*706+123_*706+124insCA
ENST00000539553.6:c.2558+123_2558+124insCA ENSP00000441370.1:n.2558+123_2558+124insCA
NM_001174089.1:c.2558+123_2558+124insCA NP_001167560.1:n.2558+123_2558+124insCA
NM_001174090.1:c.2687+123_2687+124insCA NP_001167561.1:n.2687+123_2687+124insCA
NM_032034.3:c.2606+123_2606+124insCA NP_114423.1:n.2606+123_2606+124insCA
XM_005260856.3:c.2927+123_2927+124insCA XP_005260913.1:n.2927+123_2927+124insCA
XM_005260857.1:c.2501+123_2501+124insCA XP_005260914.1:n.2501+123_2501+124insCA
XM_011529383.1:c.2525+123_2525+124insCA XP_011527685.1:n.2525+123_2525+124insCA
XM_011529384.1:c.2501+123_2501+124insCA XP_011527686.1:n.2501+123_2501+124insCA
XM_011529385.1:c.2501+123_2501+124insCA XP_011527687.1:n.2501+123_2501+124insCA
XR_937167.1:n.2656+123_2656+124insCA
NM_001363745.1:c.2444+123_2444+124insCA NP_001350674.1:n.2444+123_2444+124insCA
NR_135000.1:n.2656+123_2656+124insCA
XM_005260856.5:c.2927+123_2927+124insCA XP_005260913.1:n.2927+123_2927+124insCA
XM_011529383.3:c.2525+123_2525+124insCA XP_011527685.1:n.2525+123_2525+124insCA
XM_017028093.1:c.2921+123_2921+124insCA XP_016883582.1:n.2921+123_2921+124insCA
XM_017028094.1:c.2501+123_2501+124insCA XP_016883583.1:n.2501+123_2501+124insCA
XM_017028096.1:c.2501+123_2501+124insCA XP_016883585.1:n.2501+123_2501+124insCA
XR_001754419.1:n.3101+123_3101+124insCA
XR_001754420.2:n.3081+123_3081+124insCA
NM_001174089.2:c.2558+123_2558+124insCA MANE Select NP_001167560.1:n.2558+123_2558+124insCA
NM_001363745.2:c.2444+123_2444+124insCA NP_001350674.1:n.2444+123_2444+124insCA
NM_001174090.2:c.2687+123_2687+124insCA NP_001167561.1:n.2687+123_2687+124insCA
NM_032034.4:c.2606+123_2606+124insCA NP_114423.1:n.2606+123_2606+124insCA
NM_001400277.1:c.2501+123_2501+124insCA NP_001387206.1:n.2501+123_2501+124insCA
NM_001400278.1:c.2501+123_2501+124insCA NP_001387207.1:n.2501+123_2501+124insCA
NM_001400279.1:c.2501+123_2501+124insCA NP_001387208.1:n.2501+123_2501+124insCA
NM_001400280.1:c.2573+123_2573+124insCA NP_001387209.1:n.2573+123_2573+124insCA
NR_174470.1:n.3081+123_3081+124insCA
NR_174471.1:n.3066+123_3066+124insCA