Canonical Allele Identifier: CA1590738953

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981817A= , CM000667.2:g.149981817A=	GRCh38
NC_000005.9:g.149361380A= , CM000667.1:g.149361380A=	GRCh37
NC_000005.8:g.149341573A=	NCBI36
NG_007147.2:g.22935A= , LRG_684:g.22935A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*4A= MANE Select	ENSP00000286298.4:n.*4A=
ENST00000286298.4:c.*4A=	ENSP00000286298.4:n.*4A=
ENST00000503336.1:c.372+3466A=	ENSP00000426053.1:n.372+3466A=
NM_000112.3:c.*4A= , LRG_684t1:c.*4A=	NP_000103.2:n.*4A=
XM_017009191.2:c.*4A=	XP_016864680.1:n.*4A=
NM_000112.4:c.*4A= MANE Select	NP_000103.2:n.*4A=