Canonical Allele Identifier: CA1590739042

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981997G= , CM000667.2:g.149981997G=	GRCh38
NC_000005.9:g.149361560G= , CM000667.1:g.149361560G=	GRCh37
NC_000005.8:g.149341753G=	NCBI36
NG_007147.2:g.23115G= , LRG_684:g.23115G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*184G= MANE Select	ENSP00000286298.4:n.*184G=
ENST00000286298.4:c.*184G=	ENSP00000286298.4:n.*184G=
ENST00000503336.1:c.372+3646G=	ENSP00000426053.1:n.372+3646G=
NM_000112.3:c.*184G= , LRG_684t1:c.*184G=	NP_000103.2:n.*184G=
XM_017009191.2:c.*81G=	XP_016864680.1:n.*81G=
NM_000112.4:c.*184G= MANE Select	NP_000103.2:n.*184G=