Canonical Allele Identifier: CA1590737496

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978320G= , CM000667.2:g.149978320G=	GRCh38
NC_000005.9:g.149357883G= , CM000667.1:g.149357883G=	GRCh37
NC_000005.8:g.149338076G=	NCBI36
NG_007147.2:g.19438G= , LRG_684:g.19438G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.900G=
ENST00000286298.5:c.668G= MANE Select	ENSP00000286298.4:p.Ser223=
ENST00000286298.4:c.668G=	ENSP00000286298.4:p.Ser223=
ENST00000503336.1:c.341G=	ENSP00000426053.1:p.Ser114=
NM_000112.3:c.668G= , LRG_684t1:c.668G=	NP_000103.2:p.Ser223=
XM_017009191.2:c.668G=	XP_016864680.1:p.Ser223=
NM_000112.4:c.668G= MANE Select	NP_000103.2:p.Ser223=