Canonical Allele Identifier: CA1590737435

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978165G= , CM000667.2:g.149978165G=	GRCh38
NC_000005.9:g.149357728G= , CM000667.1:g.149357728G=	GRCh37
NC_000005.8:g.149337921G=	NCBI36
NG_007147.2:g.19283G= , LRG_684:g.19283G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.745G=
ENST00000286298.5:c.513G= MANE Select	ENSP00000286298.4:p.Met171=
ENST00000286298.4:c.513G=	ENSP00000286298.4:p.Met171=
ENST00000503336.1:c.186G=	ENSP00000426053.1:p.Met62=
NM_000112.3:c.513G= , LRG_684t1:c.513G=	NP_000103.2:p.Met171=
XM_017009191.2:c.513G=	XP_016864680.1:p.Met171=
NM_000112.4:c.513G= MANE Select	NP_000103.2:p.Met171=