Canonical Allele Identifier: CA408084578

Gene: SLC4A11

Linked Data

• MyVariant Identifiers: chr20:g.3208911G>C (hg19) ; chr20:g.3228265G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3228265G>C , CM000682.2:g.3228265G>C	GRCh38
NC_000020.10:g.3208911G>C , CM000682.1:g.3208911G>C	GRCh37
NC_000020.9:g.3156911G>C	NCBI36
NG_017072.1:g.15977C>G
NG_012093.2:g.24399G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000642402.1:c.2552C>G MANE Select	ENSP00000493503.1:p.Pro851Arg
ENST00000644011.1:c.2483C>G	ENSP00000496214.1:p.Pro828Arg
ENST00000644692.1:c.2351C>G	ENSP00000493824.1:p.Pro784Arg
ENST00000647296.1:c.2438C>G	ENSP00000495050.1:p.Pro813Arg
ENST00000380056.7:c.2600C>G	ENSP00000369396.3:p.Pro867Arg
ENST00000380059.7:c.2681C>G	ENSP00000369399.3:p.Pro894Arg
ENST00000474451.5:c.*700C>G	ENSP00000476859.1:n.*700C>G
ENST00000539553.6:c.2552C>G	ENSP00000441370.1:p.Pro851Arg
NM_001174089.1:c.2552C>G	NP_001167560.1:p.Pro851Arg
NM_001174090.1:c.2681C>G	NP_001167561.1:p.Pro894Arg
NM_032034.3:c.2600C>G	NP_114423.1:p.Pro867Arg
XM_005260856.3:c.2921C>G	XP_005260913.1:p.Pro974Arg
XM_005260857.1:c.2495C>G	XP_005260914.1:p.Pro832Arg
XM_011529383.1:c.2519C>G	XP_011527685.1:p.Pro840Arg
XM_011529384.1:c.2495C>G	XP_011527686.1:p.Pro832Arg
XM_011529385.1:c.2495C>G	XP_011527687.1:p.Pro832Arg
XR_937167.1:n.2650C>G
NM_001363745.1:c.2438C>G	NP_001350674.1:p.Pro813Arg
NR_135000.1:n.2650C>G
XM_005260856.5:c.2921C>G	XP_005260913.1:p.Pro974Arg
XM_011529383.3:c.2519C>G	XP_011527685.1:p.Pro840Arg
XM_017028093.1:c.2915C>G	XP_016883582.1:p.Pro972Arg
XM_017028094.1:c.2495C>G	XP_016883583.1:p.Pro832Arg
XM_017028096.1:c.2495C>G	XP_016883585.1:p.Pro832Arg
XR_001754419.1:n.3095C>G
XR_001754420.2:n.3075C>G
NM_001174089.2:c.2552C>G MANE Select	NP_001167560.1:p.Pro851Arg
NM_001363745.2:c.2438C>G	NP_001350674.1:p.Pro813Arg
NM_001174090.2:c.2681C>G	NP_001167561.1:p.Pro894Arg
NM_032034.4:c.2600C>G	NP_114423.1:p.Pro867Arg
NM_001400277.1:c.2495C>G	NP_001387206.1:p.Pro832Arg
NM_001400278.1:c.2495C>G	NP_001387207.1:p.Pro832Arg
NM_001400279.1:c.2495C>G	NP_001387208.1:p.Pro832Arg
NM_001400280.1:c.2567C>G	NP_001387209.1:p.Pro856Arg
NR_174470.1:n.3075C>G
NR_174471.1:n.3060C>G