Canonical Allele Identifier: CA1590738279

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149980264_149980265delinsAT , CM000667.2:g.149980264_149980265delinsAT	GRCh38
NC_000005.9:g.149359827_149359828delinsAT , CM000667.1:g.149359827_149359828delinsAT	GRCh37
NC_000005.8:g.149340020_149340021delinsAT	NCBI36
NG_007147.2:g.21382_21383delinsAT , LRG_684:g.21382_21383delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.700-29_700-28delinsAT MANE Select	ENSP00000286298.4:n.700-29_700-28delinsAT
ENST00000286298.4:c.700-29_700-28delinsAT	ENSP00000286298.4:n.700-29_700-28delinsAT
ENST00000503336.1:c.372+1913_372+1914delinsAT	ENSP00000426053.1:n.372+1913_372+1914delinsAT
NM_000112.3:c.700-29_700-28delinsAT , LRG_684t1:c.700-29_700-28delinsAT	NP_000103.2:n.700-29_700-28delinsAT
XM_017009191.2:c.700-29_700-28delinsAT	XP_016864680.1:n.700-29_700-28delinsAT
NM_000112.4:c.700-29_700-28delinsAT MANE Select	NP_000103.2:n.700-29_700-28delinsAT