Canonical Allele Identifier: CA1590738984

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981866C= , CM000667.2:g.149981866C=	GRCh38
NC_000005.9:g.149361429C= , CM000667.1:g.149361429C=	GRCh37
NC_000005.8:g.149341622C=	NCBI36
NG_007147.2:g.22984C= , LRG_684:g.22984C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*53C= MANE Select	ENSP00000286298.4:n.*53C=
ENST00000286298.4:c.*53C=	ENSP00000286298.4:n.*53C=
ENST00000503336.1:c.372+3515C=	ENSP00000426053.1:n.372+3515C=
NM_000112.3:c.*53C= , LRG_684t1:c.*53C=	NP_000103.2:n.*53C=
XM_017009191.2:c.*12+41C=	XP_016864680.1:n.*12+41C=
NM_000112.4:c.*53C= MANE Select	NP_000103.2:n.*53C=