Canonical Allele Identifier: CA1590737469

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978229T= , CM000667.2:g.149978229T=	GRCh38
NC_000005.9:g.149357792T= , CM000667.1:g.149357792T=	GRCh37
NC_000005.8:g.149337985T=	NCBI36
NG_007147.2:g.19347T= , LRG_684:g.19347T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.809T=
ENST00000286298.5:c.577T= MANE Select	ENSP00000286298.4:p.Ser193=
ENST00000286298.4:c.577T=	ENSP00000286298.4:p.Ser193=
ENST00000503336.1:c.250T=	ENSP00000426053.1:p.Ser84=
NM_000112.3:c.577T= , LRG_684t1:c.577T=	NP_000103.2:p.Ser193=
XM_017009191.2:c.577T=	XP_016864680.1:p.Ser193=
NM_000112.4:c.577T= MANE Select	NP_000103.2:p.Ser193=