Canonical Allele Identifier: CA1590737272

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149977759G= , CM000667.2:g.149977759G=	GRCh38
NC_000005.9:g.149357322G= , CM000667.1:g.149357322G=	GRCh37
NC_000005.8:g.149337515G=	NCBI36
NG_007147.2:g.18877G= , LRG_684:g.18877G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000690410.1:n.339G=
ENST00000286298.5:c.107G= MANE Select	ENSP00000286298.4:p.Ser36=
ENST00000286298.4:c.107G=	ENSP00000286298.4:p.Ser36=
NM_000112.3:c.107G= , LRG_684t1:c.107G=	NP_000103.2:p.Ser36=
XM_017009191.2:c.107G=	XP_016864680.1:p.Ser36=
NM_000112.4:c.107G= MANE Select	NP_000103.2:p.Ser36=