Canonical Allele Identifier: CA1590738962

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981831A= , CM000667.2:g.149981831A=	GRCh38
NC_000005.9:g.149361394A= , CM000667.1:g.149361394A=	GRCh37
NC_000005.8:g.149341587A=	NCBI36
NG_007147.2:g.22949A= , LRG_684:g.22949A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*18A= MANE Select	ENSP00000286298.4:n.*18A=
ENST00000286298.4:c.*18A=	ENSP00000286298.4:n.*18A=
ENST00000503336.1:c.372+3480A=	ENSP00000426053.1:n.372+3480A=
NM_000112.3:c.*18A= , LRG_684t1:c.*18A=	NP_000103.2:n.*18A=
XM_017009191.2:c.*12+6A=	XP_016864680.1:n.*12+6A=
NM_000112.4:c.*18A= MANE Select	NP_000103.2:n.*18A=