Canonical Allele Identifier: CA2651690991

Gene: SLC4A11

Linked Data

• gnomAD v4: 20-3228135-C-CCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3228135_3228136insCCG , CM000682.2:g.3228135_3228136insCCG	GRCh38
NC_000020.10:g.3208781_3208782insCCG , CM000682.1:g.3208781_3208782insCCG	GRCh37
NC_000020.9:g.3156781_3156782insCCG	NCBI36
NG_017072.1:g.16106_16107insCGG
NG_012093.2:g.24269_24270insCCG

Transcript Alleles

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