Canonical Allele Identifier: CA2346474927

Gene: SLC4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3228299T= , CM000682.2:g.3228299T=	GRCh38
NC_000020.10:g.3208945T= , CM000682.1:g.3208945T=	GRCh37
NC_000020.9:g.3156945T=	NCBI36
NG_017072.1:g.15943A=
NG_012093.2:g.24433T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001174089.2:c.2518A= MANE Select	NP_001167560.1:p.Met840=
ENST00000642402.1:c.2518A= MANE Select	ENSP00000493503.1:p.Met840=
NM_001174089.1:c.2518A=	NP_001167560.1:p.Met840=
NM_001174090.1:c.2647A=	NP_001167561.1:p.Met883=
NM_001174090.2:c.2647A=	NP_001167561.1:p.Met883=
NM_001363745.1:c.2404A=	NP_001350674.1:p.Met802=
NM_001363745.2:c.2404A=	NP_001350674.1:p.Met802=
NM_001400277.1:c.2461A=	NP_001387206.1:p.Met821=
NM_001400278.1:c.2461A=	NP_001387207.1:p.Met821=
NM_001400279.1:c.2461A=	NP_001387208.1:p.Met821=
NM_001400280.1:c.2533A=	NP_001387209.1:p.Met845=
NM_032034.3:c.2566A=	NP_114423.1:p.Met856=
NM_032034.4:c.2566A=	NP_114423.1:p.Met856=
NR_135000.1:n.2616A=
NR_174470.1:n.3041A=
NR_174471.1:n.3026A=
ENST00000380056.7:c.2566A=	ENSP00000369396.3:p.Met856=
ENST00000380059.7:c.2647A=	ENSP00000369399.3:p.Met883=
ENST00000474451.5:c.*666A=	ENSP00000476859.1:n.*666A=
ENST00000539553.6:c.2518A=	ENSP00000441370.1:p.Met840=
ENST00000644011.1:c.2449A=	ENSP00000496214.1:p.Met817=
ENST00000644692.1:c.2317A=	ENSP00000493824.1:p.Met773=
ENST00000647296.1:c.2404A=	ENSP00000495050.1:p.Met802=
XM_005260856.3:c.2887A=	XP_005260913.1:p.Met963=
XM_005260856.5:c.2887A=	XP_005260913.1:p.Met963=
XM_005260857.1:c.2461A=	XP_005260914.1:p.Met821=
XM_011529383.1:c.2485A=	XP_011527685.1:p.Met829=
XM_011529383.3:c.2485A=	XP_011527685.1:p.Met829=
XM_011529384.1:c.2461A=	XP_011527686.1:p.Met821=
XM_011529385.1:c.2461A=	XP_011527687.1:p.Met821=
XM_017028093.1:c.2881A=	XP_016883582.1:p.Met961=
XM_017028094.1:c.2461A=	XP_016883583.1:p.Met821=
XM_017028096.1:c.2461A=	XP_016883585.1:p.Met821=
XR_001754419.1:n.3061A=
XR_001754420.2:n.3041A=
XR_937167.1:n.2616A=