Canonical Allele Identifier: CA1590738848

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981595A= , CM000667.2:g.149981595A=	GRCh38
NC_000005.9:g.149361158A= , CM000667.1:g.149361158A=	GRCh37
NC_000005.8:g.149341351A=	NCBI36
NG_007147.2:g.22713A= , LRG_684:g.22713A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.2002A= MANE Select	ENSP00000286298.4:p.Lys668=
ENST00000286298.4:c.2002A=	ENSP00000286298.4:p.Lys668=
ENST00000503336.1:c.372+3244A=	ENSP00000426053.1:n.372+3244A=
NM_000112.3:c.2002A= , LRG_684t1:c.2002A=	NP_000103.2:p.Lys668=
XM_017009191.2:c.2002A=	XP_016864680.1:p.Lys668=
NM_000112.4:c.2002A= MANE Select	NP_000103.2:p.Lys668=