Canonical Allele Identifier: CA2651690973

Gene: SLC4A11

Linked Data

• gnomAD v4: 20-3228134-G-GCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3228135_3228136insCCCCCCC , CM000682.2:g.3228135_3228136insCCCCCCC	GRCh38
NC_000020.10:g.3208781_3208782insCCCCCCC , CM000682.1:g.3208781_3208782insCCCCCCC	GRCh37
NC_000020.9:g.3156781_3156782insCCCCCCC	NCBI36
NG_017072.1:g.16107_16108insGGGGGGG
NG_012093.2:g.24269_24270insCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642402.1:c.2558+124_2558+125insGGGGGGG MANE Select	ENSP00000493503.1:n.2558+124_2558+125insGGGGGGG
ENST00000644011.1:c.2489+124_2489+125insGGGGGGG	ENSP00000496214.1:n.2489+124_2489+125insGGGGGGG
ENST00000644692.1:c.2357+124_2357+125insGGGGGGG	ENSP00000493824.1:n.2357+124_2357+125insGGGGGGG
ENST00000647296.1:c.2444+124_2444+125insGGGGGGG	ENSP00000495050.1:n.2444+124_2444+125insGGGGGGG
ENST00000380056.7:c.2606+124_2606+125insGGGGGGG	ENSP00000369396.3:n.2606+124_2606+125insGGGGGGG
ENST00000380059.7:c.2687+124_2687+125insGGGGGGG	ENSP00000369399.3:n.2687+124_2687+125insGGGGGGG
ENST00000474451.5:c.*706+124_*706+125insGGGGGGG	ENSP00000476859.1:n.*706+124_*706+125insGGGGGGG
ENST00000539553.6:c.2558+124_2558+125insGGGGGGG	ENSP00000441370.1:n.2558+124_2558+125insGGGGGGG
NM_001174089.1:c.2558+124_2558+125insGGGGGGG	NP_001167560.1:n.2558+124_2558+125insGGGGGGG
NM_001174090.1:c.2687+124_2687+125insGGGGGGG	NP_001167561.1:n.2687+124_2687+125insGGGGGGG
NM_032034.3:c.2606+124_2606+125insGGGGGGG	NP_114423.1:n.2606+124_2606+125insGGGGGGG
XM_005260856.3:c.2927+124_2927+125insGGGGGGG	XP_005260913.1:n.2927+124_2927+125insGGGGGGG
XM_005260857.1:c.2501+124_2501+125insGGGGGGG	XP_005260914.1:n.2501+124_2501+125insGGGGGGG
XM_011529383.1:c.2525+124_2525+125insGGGGGGG	XP_011527685.1:n.2525+124_2525+125insGGGGGGG
XM_011529384.1:c.2501+124_2501+125insGGGGGGG	XP_011527686.1:n.2501+124_2501+125insGGGGGGG
XM_011529385.1:c.2501+124_2501+125insGGGGGGG	XP_011527687.1:n.2501+124_2501+125insGGGGGGG
XR_937167.1:n.2656+124_2656+125insGGGGGGG
NM_001363745.1:c.2444+124_2444+125insGGGGGGG	NP_001350674.1:n.2444+124_2444+125insGGGGGGG
NR_135000.1:n.2656+124_2656+125insGGGGGGG
XM_005260856.5:c.2927+124_2927+125insGGGGGGG	XP_005260913.1:n.2927+124_2927+125insGGGGGGG
XM_011529383.3:c.2525+124_2525+125insGGGGGGG	XP_011527685.1:n.2525+124_2525+125insGGGGGGG
XM_017028093.1:c.2921+124_2921+125insGGGGGGG	XP_016883582.1:n.2921+124_2921+125insGGGGGGG
XM_017028094.1:c.2501+124_2501+125insGGGGGGG	XP_016883583.1:n.2501+124_2501+125insGGGGGGG
XM_017028096.1:c.2501+124_2501+125insGGGGGGG	XP_016883585.1:n.2501+124_2501+125insGGGGGGG
XR_001754419.1:n.3101+124_3101+125insGGGGGGG
XR_001754420.2:n.3081+124_3081+125insGGGGGGG
NM_001174089.2:c.2558+124_2558+125insGGGGGGG MANE Select	NP_001167560.1:n.2558+124_2558+125insGGGGGGG
NM_001363745.2:c.2444+124_2444+125insGGGGGGG	NP_001350674.1:n.2444+124_2444+125insGGGGGGG
NM_001174090.2:c.2687+124_2687+125insGGGGGGG	NP_001167561.1:n.2687+124_2687+125insGGGGGGG
NM_032034.4:c.2606+124_2606+125insGGGGGGG	NP_114423.1:n.2606+124_2606+125insGGGGGGG
NM_001400277.1:c.2501+124_2501+125insGGGGGGG	NP_001387206.1:n.2501+124_2501+125insGGGGGGG
NM_001400278.1:c.2501+124_2501+125insGGGGGGG	NP_001387207.1:n.2501+124_2501+125insGGGGGGG
NM_001400279.1:c.2501+124_2501+125insGGGGGGG	NP_001387208.1:n.2501+124_2501+125insGGGGGGG
NM_001400280.1:c.2573+124_2573+125insGGGGGGG	NP_001387209.1:n.2573+124_2573+125insGGGGGGG
NR_174470.1:n.3081+124_3081+125insGGGGGGG
NR_174471.1:n.3066+124_3066+125insGGGGGGG