Canonical Allele Identifier: CA2651691082

Gene: SLC4A11

Linked Data

• gnomAD v4: 20-3228146-A-ACC

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3228148_3228149dup , CM000682.2:g.3228148_3228149dup	GRCh38
NC_000020.10:g.3208794_3208795dup , CM000682.1:g.3208794_3208795dup	GRCh37
NC_000020.9:g.3156794_3156795dup	NCBI36
NG_017072.1:g.16094_16095dup
NG_012093.2:g.24282_24283dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642402.1:c.2558+111_2558+112dup MANE Select	ENSP00000493503.1:n.2558+111_2558+112dup
ENST00000644011.1:c.2489+111_2489+112dup	ENSP00000496214.1:n.2489+111_2489+112dup
ENST00000644692.1:c.2357+111_2357+112dup	ENSP00000493824.1:n.2357+111_2357+112dup
ENST00000647296.1:c.2444+111_2444+112dup	ENSP00000495050.1:n.2444+111_2444+112dup
ENST00000380056.7:c.2606+111_2606+112dup	ENSP00000369396.3:n.2606+111_2606+112dup
ENST00000380059.7:c.2687+111_2687+112dup	ENSP00000369399.3:n.2687+111_2687+112dup
ENST00000474451.5:c.*706+111_*706+112dup	ENSP00000476859.1:n.*706+111_*706+112dup
ENST00000539553.6:c.2558+111_2558+112dup	ENSP00000441370.1:n.2558+111_2558+112dup
NM_001174089.1:c.2558+111_2558+112dup	NP_001167560.1:n.2558+111_2558+112dup
NM_001174090.1:c.2687+111_2687+112dup	NP_001167561.1:n.2687+111_2687+112dup
NM_032034.3:c.2606+111_2606+112dup	NP_114423.1:n.2606+111_2606+112dup
XM_005260856.3:c.2927+111_2927+112dup	XP_005260913.1:n.2927+111_2927+112dup
XM_005260857.1:c.2501+111_2501+112dup	XP_005260914.1:n.2501+111_2501+112dup
XM_011529383.1:c.2525+111_2525+112dup	XP_011527685.1:n.2525+111_2525+112dup
XM_011529384.1:c.2501+111_2501+112dup	XP_011527686.1:n.2501+111_2501+112dup
XM_011529385.1:c.2501+111_2501+112dup	XP_011527687.1:n.2501+111_2501+112dup
XR_937167.1:n.2656+111_2656+112dup
NM_001363745.1:c.2444+111_2444+112dup	NP_001350674.1:n.2444+111_2444+112dup
NR_135000.1:n.2656+111_2656+112dup
XM_005260856.5:c.2927+111_2927+112dup	XP_005260913.1:n.2927+111_2927+112dup
XM_011529383.3:c.2525+111_2525+112dup	XP_011527685.1:n.2525+111_2525+112dup
XM_017028093.1:c.2921+111_2921+112dup	XP_016883582.1:n.2921+111_2921+112dup
XM_017028094.1:c.2501+111_2501+112dup	XP_016883583.1:n.2501+111_2501+112dup
XM_017028096.1:c.2501+111_2501+112dup	XP_016883585.1:n.2501+111_2501+112dup
XR_001754419.1:n.3101+111_3101+112dup
XR_001754420.2:n.3081+111_3081+112dup
NM_001174089.2:c.2558+111_2558+112dup MANE Select	NP_001167560.1:n.2558+111_2558+112dup
NM_001363745.2:c.2444+111_2444+112dup	NP_001350674.1:n.2444+111_2444+112dup
NM_001174090.2:c.2687+111_2687+112dup	NP_001167561.1:n.2687+111_2687+112dup
NM_032034.4:c.2606+111_2606+112dup	NP_114423.1:n.2606+111_2606+112dup
NM_001400277.1:c.2501+111_2501+112dup	NP_001387206.1:n.2501+111_2501+112dup
NM_001400278.1:c.2501+111_2501+112dup	NP_001387207.1:n.2501+111_2501+112dup
NM_001400279.1:c.2501+111_2501+112dup	NP_001387208.1:n.2501+111_2501+112dup
NM_001400280.1:c.2573+111_2573+112dup	NP_001387209.1:n.2573+111_2573+112dup
NR_174470.1:n.3081+111_3081+112dup
NR_174471.1:n.3066+111_3066+112dup