Canonical Allele Identifier: CA509559230

Gene: SLC4A11

Linked Data

• MyVariant Identifiers: chr20:g.3214925A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3234279A>T , CM000682.2:g.3234279A>T	GRCh38
NC_000020.10:g.3214925A>T , CM000682.1:g.3214925A>T	GRCh37
NC_000020.9:g.3162925A>T	NCBI36
NG_017072.1:g.9963T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642402.1:c.327T>A MANE Select	ENSP00000493503.1:p.Arg109=
ENST00000644011.1:c.292-34T>A	ENSP00000496214.1:n.292-34T>A
ENST00000644692.1:c.270T>A	ENSP00000493824.1:p.Arg90=
ENST00000645524.1:c.*239T>A	ENSP00000495635.1:n.*239T>A
ENST00000647296.1:c.327T>A	ENSP00000495050.1:p.Arg109=
ENST00000380056.7:c.375T>A	ENSP00000369396.3:p.Arg125=
ENST00000380059.7:c.456T>A	ENSP00000369399.3:p.Arg152=
ENST00000437836.2:c.270T>A	ENSP00000404271.2:p.Arg90=
ENST00000474451.5:c.270T>A	ENSP00000476859.1:p.Arg90=
ENST00000539553.6:c.327T>A	ENSP00000441370.1:p.Arg109=
NM_001174089.1:c.327T>A	NP_001167560.1:p.Arg109=
NM_001174090.1:c.456T>A	NP_001167561.1:p.Arg152=
NM_032034.3:c.375T>A	NP_114423.1:p.Arg125=
XM_005260856.3:c.810T>A	XP_005260913.1:p.Arg270=
XM_005260857.1:c.270T>A	XP_005260914.1:p.Arg90=
XM_011529383.1:c.294T>A	XP_011527685.1:p.Arg98=
XM_011529384.1:c.270T>A	XP_011527686.1:p.Arg90=
XM_011529385.1:c.270T>A	XP_011527687.1:p.Arg90=
XM_011529386.1:c.810T>A	XP_011527688.1:p.Arg270=
XR_937167.1:n.495T>A
NM_001363745.1:c.327T>A	NP_001350674.1:p.Arg109=
NR_135000.1:n.495T>A
XM_005260856.5:c.810T>A	XP_005260913.1:p.Arg270=
XM_011529383.3:c.294T>A	XP_011527685.1:p.Arg98=
XM_017028093.1:c.810T>A	XP_016883582.1:p.Arg270=
XM_017028094.1:c.270T>A	XP_016883583.1:p.Arg90=
XM_017028096.1:c.270T>A	XP_016883585.1:p.Arg90=
XM_017028097.1:c.810T>A	XP_016883586.1:p.Arg270=
XR_001754419.1:n.920T>A
XR_001754420.2:n.920T>A
NM_001174089.2:c.327T>A MANE Select	NP_001167560.1:p.Arg109=
NM_001363745.2:c.327T>A	NP_001350674.1:p.Arg109=
NM_001174090.2:c.456T>A	NP_001167561.1:p.Arg152=
NM_032034.4:c.375T>A	NP_114423.1:p.Arg125=
NM_001400277.1:c.270T>A	NP_001387206.1:p.Arg90=
NM_001400278.1:c.270T>A	NP_001387207.1:p.Arg90=
NM_001400279.1:c.270T>A	NP_001387208.1:p.Arg90=
NM_001400280.1:c.456T>A	NP_001387209.1:p.Arg152=
NR_174470.1:n.885T>A
NR_174471.1:n.885T>A