Canonical Allele Identifier: CA1590739039

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981986G= , CM000667.2:g.149981986G=	GRCh38
NC_000005.9:g.149361549G= , CM000667.1:g.149361549G=	GRCh37
NC_000005.8:g.149341742G=	NCBI36
NG_007147.2:g.23104G= , LRG_684:g.23104G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*173G= MANE Select	ENSP00000286298.4:n.*173G=
ENST00000286298.4:c.*173G=	ENSP00000286298.4:n.*173G=
ENST00000503336.1:c.372+3635G=	ENSP00000426053.1:n.372+3635G=
NM_000112.3:c.*173G= , LRG_684t1:c.*173G=	NP_000103.2:n.*173G=
XM_017009191.2:c.*70G=	XP_016864680.1:n.*70G=
NM_000112.4:c.*173G= MANE Select	NP_000103.2:n.*173G=