Canonical Allele Identifier: CA1590738961

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981829G= , CM000667.2:g.149981829G=	GRCh38
NC_000005.9:g.149361392G= , CM000667.1:g.149361392G=	GRCh37
NC_000005.8:g.149341585G=	NCBI36
NG_007147.2:g.22947G= , LRG_684:g.22947G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*16G= MANE Select	ENSP00000286298.4:n.*16G=
ENST00000286298.4:c.*16G=	ENSP00000286298.4:n.*16G=
ENST00000503336.1:c.372+3478G=	ENSP00000426053.1:n.372+3478G=
NM_000112.3:c.*16G= , LRG_684t1:c.*16G=	NP_000103.2:n.*16G=
XM_017009191.2:c.*12+4G=	XP_016864680.1:n.*12+4G=
NM_000112.4:c.*16G= MANE Select	NP_000103.2:n.*16G=