Canonical Allele Identifier: CA1590739017

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981948G= , CM000667.2:g.149981948G=	GRCh38
NC_000005.9:g.149361511G= , CM000667.1:g.149361511G=	GRCh37
NC_000005.8:g.149341704G=	NCBI36
NG_007147.2:g.23066G= , LRG_684:g.23066G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*135G= MANE Select	ENSP00000286298.4:n.*135G=
ENST00000286298.4:c.*135G=	ENSP00000286298.4:n.*135G=
ENST00000503336.1:c.372+3597G=	ENSP00000426053.1:n.372+3597G=
NM_000112.3:c.*135G= , LRG_684t1:c.*135G=	NP_000103.2:n.*135G=
XM_017009191.2:c.*32G=	XP_016864680.1:n.*32G=
NM_000112.4:c.*135G= MANE Select	NP_000103.2:n.*135G=