Canonical Allele Identifier: CA2346477993

Gene: SLC4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3234193G= , CM000682.2:g.3234193G=	GRCh38
NC_000020.10:g.3214839G= , CM000682.1:g.3214839G=	GRCh37
NC_000020.9:g.3162839G=	NCBI36
NG_017072.1:g.10049C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642402.1:c.413C= MANE Select	ENSP00000493503.1:p.Thr138=
ENST00000644011.1:c.344C=	ENSP00000496214.1:p.Thr115=
ENST00000644692.1:c.356C=	ENSP00000493824.1:p.Thr119=
ENST00000647296.1:c.413C=	ENSP00000495050.1:p.Thr138=
ENST00000380056.7:c.461C=	ENSP00000369396.3:p.Thr154=
ENST00000380059.7:c.542C=	ENSP00000369399.3:p.Thr181=
ENST00000474451.5:c.356C=	ENSP00000476859.1:p.Thr119=
ENST00000539553.6:c.413C=	ENSP00000441370.1:p.Thr138=
NM_001174089.1:c.413C=	NP_001167560.1:p.Thr138=
NM_001174090.1:c.542C=	NP_001167561.1:p.Thr181=
NM_032034.3:c.461C=	NP_114423.1:p.Thr154=
XM_005260856.3:c.896C=	XP_005260913.1:p.Thr299=
XM_005260857.1:c.356C=	XP_005260914.1:p.Thr119=
XM_011529383.1:c.380C=	XP_011527685.1:p.Thr127=
XM_011529384.1:c.356C=	XP_011527686.1:p.Thr119=
XM_011529385.1:c.356C=	XP_011527687.1:p.Thr119=
XM_011529386.1:c.896C=	XP_011527688.1:p.Thr299=
XR_937167.1:n.581C=
NM_001363745.1:c.413C=	NP_001350674.1:p.Thr138=
NR_135000.1:n.581C=
XM_005260856.5:c.896C=	XP_005260913.1:p.Thr299=
XM_011529383.3:c.380C=	XP_011527685.1:p.Thr127=
XM_017028093.1:c.896C=	XP_016883582.1:p.Thr299=
XM_017028094.1:c.356C=	XP_016883583.1:p.Thr119=
XM_017028096.1:c.356C=	XP_016883585.1:p.Thr119=
XM_017028097.1:c.896C=	XP_016883586.1:p.Thr299=
XR_001754419.1:n.1006C=
XR_001754420.2:n.1006C=
NM_001174089.2:c.413C= MANE Select	NP_001167560.1:p.Thr138=
NM_001363745.2:c.413C=	NP_001350674.1:p.Thr138=
NM_001174090.2:c.542C=	NP_001167561.1:p.Thr181=
NM_032034.4:c.461C=	NP_114423.1:p.Thr154=
NM_001400277.1:c.356C=	NP_001387206.1:p.Thr119=
NM_001400278.1:c.356C=	NP_001387207.1:p.Thr119=
NM_001400279.1:c.356C=	NP_001387208.1:p.Thr119=
NM_001400280.1:c.542C=	NP_001387209.1:p.Thr181=
NR_174470.1:n.971C=
NR_174471.1:n.971C=