Canonical Allele Identifier: CA1590739040

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981994A= , CM000667.2:g.149981994A=	GRCh38
NC_000005.9:g.149361557A= , CM000667.1:g.149361557A=	GRCh37
NC_000005.8:g.149341750A=	NCBI36
NG_007147.2:g.23112A= , LRG_684:g.23112A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*181A= MANE Select	ENSP00000286298.4:n.*181A=
ENST00000286298.4:c.*181A=	ENSP00000286298.4:n.*181A=
ENST00000503336.1:c.372+3643A=	ENSP00000426053.1:n.372+3643A=
NM_000112.3:c.*181A= , LRG_684t1:c.*181A=	NP_000103.2:n.*181A=
XM_017009191.2:c.*78A=	XP_016864680.1:n.*78A=
NM_000112.4:c.*181A= MANE Select	NP_000103.2:n.*181A=