Canonical Allele Identifier: CA1590737494

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978310A= , CM000667.2:g.149978310A=	GRCh38
NC_000005.9:g.149357873A= , CM000667.1:g.149357873A=	GRCh37
NC_000005.8:g.149338066A=	NCBI36
NG_007147.2:g.19428A= , LRG_684:g.19428A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.890A=
ENST00000286298.5:c.658A= MANE Select	ENSP00000286298.4:p.Met220=
ENST00000286298.4:c.658A=	ENSP00000286298.4:p.Met220=
ENST00000503336.1:c.331A=	ENSP00000426053.1:p.Met111=
NM_000112.3:c.658A= , LRG_684t1:c.658A=	NP_000103.2:p.Met220=
XM_017009191.2:c.658A=	XP_016864680.1:p.Met220=
NM_000112.4:c.658A= MANE Select	NP_000103.2:p.Met220=