Canonical Allele Identifier: CA1014849447

Gene: SLC4A11

Linked Data

• gnomAD v3: 20-3228068-TCCTCCTGCCCGCCAGCCTCCCCAGCCCGCCCACTCTCCACCCCTAGGCAGGACC-T
• gnomAD v4: 20-3228068-TCCTCCTGCCCGCCAGCCTCCCCAGCCCGCCCACTCTCCACCCCTAGGCAGGACC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3228075_3228128del , CM000682.2:g.3228075_3228128del	GRCh38
NC_000020.10:g.3208721_3208774del , CM000682.1:g.3208721_3208774del	GRCh37
NC_000020.9:g.3156721_3156774del	NCBI36
NG_017072.1:g.16120_16173del
NG_012093.2:g.24209_24262del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642402.1:c.2558+137_2558+190del MANE Select	ENSP00000493503.1:n.2558+137_2558+190del
ENST00000644011.1:c.2489+137_2489+190del	ENSP00000496214.1:n.2489+137_2489+190del
ENST00000644692.1:c.2357+137_2357+190del	ENSP00000493824.1:n.2357+137_2357+190del
ENST00000647296.1:c.2444+137_2444+190del	ENSP00000495050.1:n.2444+137_2444+190del
ENST00000380056.7:c.2606+137_2606+190del	ENSP00000369396.3:n.2606+137_2606+190del
ENST00000380059.7:c.2687+137_2687+190del	ENSP00000369399.3:n.2687+137_2687+190del
ENST00000474451.5:c.*706+137_*706+190del	ENSP00000476859.1:n.*706+137_*706+190del
ENST00000539553.6:c.2558+137_2558+190del	ENSP00000441370.1:n.2558+137_2558+190del
NM_001174089.1:c.2558+137_2558+190del	NP_001167560.1:n.2558+137_2558+190del
NM_001174090.1:c.2687+137_2687+190del	NP_001167561.1:n.2687+137_2687+190del
NM_032034.3:c.2606+137_2606+190del	NP_114423.1:n.2606+137_2606+190del
XM_005260856.3:c.2927+137_2927+190del	XP_005260913.1:n.2927+137_2927+190del
XM_005260857.1:c.2501+137_2501+190del	XP_005260914.1:n.2501+137_2501+190del
XM_011529383.1:c.2525+137_2525+190del	XP_011527685.1:n.2525+137_2525+190del
XM_011529384.1:c.2501+137_2501+190del	XP_011527686.1:n.2501+137_2501+190del
XM_011529385.1:c.2501+137_2501+190del	XP_011527687.1:n.2501+137_2501+190del
XR_937167.1:n.2656+137_2656+190del
NM_001363745.1:c.2444+137_2444+190del	NP_001350674.1:n.2444+137_2444+190del
NR_135000.1:n.2656+137_2656+190del
XM_005260856.5:c.2927+137_2927+190del	XP_005260913.1:n.2927+137_2927+190del
XM_011529383.3:c.2525+137_2525+190del	XP_011527685.1:n.2525+137_2525+190del
XM_017028093.1:c.2921+137_2921+190del	XP_016883582.1:n.2921+137_2921+190del
XM_017028094.1:c.2501+137_2501+190del	XP_016883583.1:n.2501+137_2501+190del
XM_017028096.1:c.2501+137_2501+190del	XP_016883585.1:n.2501+137_2501+190del
XR_001754419.1:n.3101+137_3101+190del
XR_001754420.2:n.3081+137_3081+190del
NM_001174089.2:c.2558+137_2558+190del MANE Select	NP_001167560.1:n.2558+137_2558+190del
NM_001363745.2:c.2444+137_2444+190del	NP_001350674.1:n.2444+137_2444+190del
NM_001174090.2:c.2687+137_2687+190del	NP_001167561.1:n.2687+137_2687+190del
NM_032034.4:c.2606+137_2606+190del	NP_114423.1:n.2606+137_2606+190del
NM_001400277.1:c.2501+137_2501+190del	NP_001387206.1:n.2501+137_2501+190del
NM_001400278.1:c.2501+137_2501+190del	NP_001387207.1:n.2501+137_2501+190del
NM_001400279.1:c.2501+137_2501+190del	NP_001387208.1:n.2501+137_2501+190del
NM_001400280.1:c.2573+137_2573+190del	NP_001387209.1:n.2573+137_2573+190del
NR_174470.1:n.3081+137_3081+190del
NR_174471.1:n.3066+137_3066+190del