Canonical Allele Identifier: CA1590738999

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981900C= , CM000667.2:g.149981900C=	GRCh38
NC_000005.9:g.149361463C= , CM000667.1:g.149361463C=	GRCh37
NC_000005.8:g.149341656C=	NCBI36
NG_007147.2:g.23018C= , LRG_684:g.23018C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*87C= MANE Select	ENSP00000286298.4:n.*87C=
ENST00000286298.4:c.*87C=	ENSP00000286298.4:n.*87C=
ENST00000503336.1:c.372+3549C=	ENSP00000426053.1:n.372+3549C=
NM_000112.3:c.*87C= , LRG_684t1:c.*87C=	NP_000103.2:n.*87C=
XM_017009191.2:c.*13-29C=	XP_016864680.1:n.*13-29C=
NM_000112.4:c.*87C= MANE Select	NP_000103.2:n.*87C=