Canonical Allele Identifier: CA1590738277

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149980263T= , CM000667.2:g.149980263T=	GRCh38
NC_000005.9:g.149359826T= , CM000667.1:g.149359826T=	GRCh37
NC_000005.8:g.149340019T=	NCBI36
NG_007147.2:g.21381T= , LRG_684:g.21381T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000286298.5:c.700-30T= MANE Select	ENSP00000286298.4:n.700-30T=
ENST00000286298.4:c.700-30T=	ENSP00000286298.4:n.700-30T=
ENST00000503336.1:c.372+1912T=	ENSP00000426053.1:n.372+1912T=
NM_000112.3:c.700-30T= , LRG_684t1:c.700-30T=	NP_000103.2:n.700-30T=
XM_017009191.2:c.700-30T=	XP_016864680.1:n.700-30T=
NM_000112.4:c.700-30T= MANE Select	NP_000103.2:n.700-30T=