Canonical Allele Identifier: CA2651691110

Gene: SLC4A11

Linked Data

• gnomAD v4: 20-3228153-C-CCCCCAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3228153_3228154insCCCCAAAA , CM000682.2:g.3228153_3228154insCCCCAAAA	GRCh38
NC_000020.10:g.3208799_3208800insCCCCAAAA , CM000682.1:g.3208799_3208800insCCCCAAAA	GRCh37
NC_000020.9:g.3156799_3156800insCCCCAAAA	NCBI36
NG_017072.1:g.16088_16089insTTTTGGGG
NG_012093.2:g.24287_24288insCCCCAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642402.1:c.2558+105_2558+106insTTTTGGGG MANE Select	ENSP00000493503.1:n.2558+105_2558+106insTTTTGGGG
ENST00000644011.1:c.2489+105_2489+106insTTTTGGGG	ENSP00000496214.1:n.2489+105_2489+106insTTTTGGGG
ENST00000644692.1:c.2357+105_2357+106insTTTTGGGG	ENSP00000493824.1:n.2357+105_2357+106insTTTTGGGG
ENST00000647296.1:c.2444+105_2444+106insTTTTGGGG	ENSP00000495050.1:n.2444+105_2444+106insTTTTGGGG
ENST00000380056.7:c.2606+105_2606+106insTTTTGGGG	ENSP00000369396.3:n.2606+105_2606+106insTTTTGGGG
ENST00000380059.7:c.2687+105_2687+106insTTTTGGGG	ENSP00000369399.3:n.2687+105_2687+106insTTTTGGGG
ENST00000474451.5:c.*706+105_*706+106insTTTTGGGG	ENSP00000476859.1:n.*706+105_*706+106insTTTTGGGG
ENST00000539553.6:c.2558+105_2558+106insTTTTGGGG	ENSP00000441370.1:n.2558+105_2558+106insTTTTGGGG
NM_001174089.1:c.2558+105_2558+106insTTTTGGGG	NP_001167560.1:n.2558+105_2558+106insTTTTGGGG
NM_001174090.1:c.2687+105_2687+106insTTTTGGGG	NP_001167561.1:n.2687+105_2687+106insTTTTGGGG
NM_032034.3:c.2606+105_2606+106insTTTTGGGG	NP_114423.1:n.2606+105_2606+106insTTTTGGGG
XM_005260856.3:c.2927+105_2927+106insTTTTGGGG	XP_005260913.1:n.2927+105_2927+106insTTTTGGGG
XM_005260857.1:c.2501+105_2501+106insTTTTGGGG	XP_005260914.1:n.2501+105_2501+106insTTTTGGGG
XM_011529383.1:c.2525+105_2525+106insTTTTGGGG	XP_011527685.1:n.2525+105_2525+106insTTTTGGGG
XM_011529384.1:c.2501+105_2501+106insTTTTGGGG	XP_011527686.1:n.2501+105_2501+106insTTTTGGGG
XM_011529385.1:c.2501+105_2501+106insTTTTGGGG	XP_011527687.1:n.2501+105_2501+106insTTTTGGGG
XR_937167.1:n.2656+105_2656+106insTTTTGGGG
NM_001363745.1:c.2444+105_2444+106insTTTTGGGG	NP_001350674.1:n.2444+105_2444+106insTTTTGGGG
NR_135000.1:n.2656+105_2656+106insTTTTGGGG
XM_005260856.5:c.2927+105_2927+106insTTTTGGGG	XP_005260913.1:n.2927+105_2927+106insTTTTGGGG
XM_011529383.3:c.2525+105_2525+106insTTTTGGGG	XP_011527685.1:n.2525+105_2525+106insTTTTGGGG
XM_017028093.1:c.2921+105_2921+106insTTTTGGGG	XP_016883582.1:n.2921+105_2921+106insTTTTGGGG
XM_017028094.1:c.2501+105_2501+106insTTTTGGGG	XP_016883583.1:n.2501+105_2501+106insTTTTGGGG
XM_017028096.1:c.2501+105_2501+106insTTTTGGGG	XP_016883585.1:n.2501+105_2501+106insTTTTGGGG
XR_001754419.1:n.3101+105_3101+106insTTTTGGGG
XR_001754420.2:n.3081+105_3081+106insTTTTGGGG
NM_001174089.2:c.2558+105_2558+106insTTTTGGGG MANE Select	NP_001167560.1:n.2558+105_2558+106insTTTTGGGG
NM_001363745.2:c.2444+105_2444+106insTTTTGGGG	NP_001350674.1:n.2444+105_2444+106insTTTTGGGG
NM_001174090.2:c.2687+105_2687+106insTTTTGGGG	NP_001167561.1:n.2687+105_2687+106insTTTTGGGG
NM_032034.4:c.2606+105_2606+106insTTTTGGGG	NP_114423.1:n.2606+105_2606+106insTTTTGGGG
NM_001400277.1:c.2501+105_2501+106insTTTTGGGG	NP_001387206.1:n.2501+105_2501+106insTTTTGGGG
NM_001400278.1:c.2501+105_2501+106insTTTTGGGG	NP_001387207.1:n.2501+105_2501+106insTTTTGGGG
NM_001400279.1:c.2501+105_2501+106insTTTTGGGG	NP_001387208.1:n.2501+105_2501+106insTTTTGGGG
NM_001400280.1:c.2573+105_2573+106insTTTTGGGG	NP_001387209.1:n.2573+105_2573+106insTTTTGGGG
NR_174470.1:n.3081+105_3081+106insTTTTGGGG
NR_174471.1:n.3066+105_3066+106insTTTTGGGG