Canonical Allele Identifier: CA9742303

Gene: SLC4A11

Linked Data

• ClinVar Variation Id: 338257
• ClinVar RCV Id: RCV000271561
• dbSNP Id: rs773524307
• ExAC: 20:3214843 G / A
• gnomAD v2: 20-3214843-G-A
• gnomAD v4: 20-3234197-G-A
• COSMIC: COSM4097695 ; COSM4097696
• MyVariant Identifiers: chr20:g.3214843G>A (hg19) ; chr20:g.3234197G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3234197G>A , CM000682.2:g.3234197G>A	GRCh38
NC_000020.10:g.3214843G>A , CM000682.1:g.3214843G>A	GRCh37
NC_000020.9:g.3162843G>A	NCBI36
NG_017072.1:g.10045C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642402.1:c.409C>T MANE Select	ENSP00000493503.1:p.Arg137Trp
ENST00000644011.1:c.340C>T	ENSP00000496214.1:p.Arg114Trp
ENST00000644692.1:c.352C>T	ENSP00000493824.1:p.Arg118Trp
ENST00000647296.1:c.409C>T	ENSP00000495050.1:p.Arg137Trp
ENST00000380056.7:c.457C>T	ENSP00000369396.3:p.Arg153Trp
ENST00000380059.7:c.538C>T	ENSP00000369399.3:p.Arg180Trp
ENST00000474451.5:c.352C>T	ENSP00000476859.1:p.Arg118Trp
ENST00000539553.6:c.409C>T	ENSP00000441370.1:p.Arg137Trp
NM_001174089.1:c.409C>T	NP_001167560.1:p.Arg137Trp
NM_001174090.1:c.538C>T	NP_001167561.1:p.Arg180Trp
NM_032034.3:c.457C>T	NP_114423.1:p.Arg153Trp
XM_005260856.3:c.892C>T	XP_005260913.1:p.Arg298Trp
XM_005260857.1:c.352C>T	XP_005260914.1:p.Arg118Trp
XM_011529383.1:c.376C>T	XP_011527685.1:p.Arg126Trp
XM_011529384.1:c.352C>T	XP_011527686.1:p.Arg118Trp
XM_011529385.1:c.352C>T	XP_011527687.1:p.Arg118Trp
XM_011529386.1:c.892C>T	XP_011527688.1:p.Arg298Trp
XR_937167.1:n.577C>T
NM_001363745.1:c.409C>T	NP_001350674.1:p.Arg137Trp
NR_135000.1:n.577C>T
XM_005260856.5:c.892C>T	XP_005260913.1:p.Arg298Trp
XM_011529383.3:c.376C>T	XP_011527685.1:p.Arg126Trp
XM_017028093.1:c.892C>T	XP_016883582.1:p.Arg298Trp
XM_017028094.1:c.352C>T	XP_016883583.1:p.Arg118Trp
XM_017028096.1:c.352C>T	XP_016883585.1:p.Arg118Trp
XM_017028097.1:c.892C>T	XP_016883586.1:p.Arg298Trp
XR_001754419.1:n.1002C>T
XR_001754420.2:n.1002C>T
NM_001174089.2:c.409C>T MANE Select	NP_001167560.1:p.Arg137Trp
NM_001363745.2:c.409C>T	NP_001350674.1:p.Arg137Trp
NM_001174090.2:c.538C>T	NP_001167561.1:p.Arg180Trp
NM_032034.4:c.457C>T	NP_114423.1:p.Arg153Trp
NM_001400277.1:c.352C>T	NP_001387206.1:p.Arg118Trp
NM_001400278.1:c.352C>T	NP_001387207.1:p.Arg118Trp
NM_001400279.1:c.352C>T	NP_001387208.1:p.Arg118Trp
NM_001400280.1:c.538C>T	NP_001387209.1:p.Arg180Trp
NR_174470.1:n.967C>T
NR_174471.1:n.967C>T