Canonical Allele Identifier: CA1590738979

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981859C= , CM000667.2:g.149981859C=	GRCh38
NC_000005.9:g.149361422C= , CM000667.1:g.149361422C=	GRCh37
NC_000005.8:g.149341615C=	NCBI36
NG_007147.2:g.22977C= , LRG_684:g.22977C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*46C= MANE Select	ENSP00000286298.4:n.*46C=
ENST00000286298.4:c.*46C=	ENSP00000286298.4:n.*46C=
ENST00000503336.1:c.372+3508C=	ENSP00000426053.1:n.372+3508C=
NM_000112.3:c.*46C= , LRG_684t1:c.*46C=	NP_000103.2:n.*46C=
XM_017009191.2:c.*12+34C=	XP_016864680.1:n.*12+34C=
NM_000112.4:c.*46C= MANE Select	NP_000103.2:n.*46C=