Canonical Allele Identifier: CA1590738627

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981047T= , CM000667.2:g.149981047T=	GRCh38
NC_000005.9:g.149360610T= , CM000667.1:g.149360610T=	GRCh37
NC_000005.8:g.149340803T=	NCBI36
NG_007147.2:g.22165T= , LRG_684:g.22165T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000286298.5:c.1454T= MANE Select	ENSP00000286298.4:p.Val485=
ENST00000286298.4:c.1454T=	ENSP00000286298.4:p.Val485=
ENST00000503336.1:c.372+2696T=	ENSP00000426053.1:n.372+2696T=
NM_000112.3:c.1454T= , LRG_684t1:c.1454T=	NP_000103.2:p.Val485=
XM_017009191.2:c.1454T=	XP_016864680.1:p.Val485=
NM_000112.4:c.1454T= MANE Select	NP_000103.2:p.Val485=