Canonical Allele Identifier: CA2346475205

Gene: SLC4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3228854C= , CM000682.2:g.3228854C=	GRCh38
NC_000020.10:g.3209500C= , CM000682.1:g.3209500C=	GRCh37
NC_000020.9:g.3157500C=	NCBI36
NG_017072.1:g.15388G=
NG_012093.2:g.24988C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000642402.1:c.2176G= MANE Select	ENSP00000493503.1:p.Gly726=
ENST00000644011.1:c.2107G=	ENSP00000496214.1:p.Gly703=
ENST00000644692.1:c.2047G=	ENSP00000493824.1:p.Gly683=
ENST00000647296.1:c.2062G=	ENSP00000495050.1:p.Gly688=
ENST00000380056.7:c.2224G=	ENSP00000369396.3:p.Gly742=
ENST00000380059.7:c.2305G=	ENSP00000369399.3:p.Gly769=
ENST00000474451.5:c.*324G=	ENSP00000476859.1:n.*324G=
ENST00000539553.6:c.2176G=	ENSP00000441370.1:p.Gly726=
NM_001174089.1:c.2176G=	NP_001167560.1:p.Gly726=
NM_001174090.1:c.2305G=	NP_001167561.1:p.Gly769=
NM_032034.3:c.2224G=	NP_114423.1:p.Gly742=
XM_005260856.3:c.2545G=	XP_005260913.1:p.Gly849=
XM_005260857.1:c.2119G=	XP_005260914.1:p.Gly707=
XM_011529383.1:c.2143G=	XP_011527685.1:p.Gly715=
XM_011529384.1:c.2119G=	XP_011527686.1:p.Gly707=
XM_011529385.1:c.2119G=	XP_011527687.1:p.Gly707=
XR_937167.1:n.2274G=
NM_001363745.1:c.2062G=	NP_001350674.1:p.Gly688=
NR_135000.1:n.2274G=
XM_005260856.5:c.2545G=	XP_005260913.1:p.Gly849=
XM_011529383.3:c.2143G=	XP_011527685.1:p.Gly715=
XM_017028093.1:c.2539G=	XP_016883582.1:p.Gly847=
XM_017028094.1:c.2119G=	XP_016883583.1:p.Gly707=
XM_017028096.1:c.2119G=	XP_016883585.1:p.Gly707=
XR_001754419.1:n.2719G=
XR_001754420.2:n.2699G=
NM_001174089.2:c.2176G= MANE Select	NP_001167560.1:p.Gly726=
NM_001363745.2:c.2062G=	NP_001350674.1:p.Gly688=
NM_001174090.2:c.2305G=	NP_001167561.1:p.Gly769=
NM_032034.4:c.2224G=	NP_114423.1:p.Gly742=
NM_001400277.1:c.2119G=	NP_001387206.1:p.Gly707=
NM_001400278.1:c.2119G=	NP_001387207.1:p.Gly707=
NM_001400279.1:c.2119G=	NP_001387208.1:p.Gly707=
NM_001400280.1:c.2191G=	NP_001387209.1:p.Gly731=
NR_174470.1:n.2699G=
NR_174471.1:n.2684G=