Canonical Allele Identifier: CA1590737477

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978263T= , CM000667.2:g.149978263T=	GRCh38
NC_000005.9:g.149357826T= , CM000667.1:g.149357826T=	GRCh37
NC_000005.8:g.149338019T=	NCBI36
NG_007147.2:g.19381T= , LRG_684:g.19381T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.843T=
ENST00000286298.5:c.611T= MANE Select	ENSP00000286298.4:p.Leu204=
ENST00000286298.4:c.611T=	ENSP00000286298.4:p.Leu204=
ENST00000503336.1:c.284T=	ENSP00000426053.1:p.Leu95=
NM_000112.3:c.611T= , LRG_684t1:c.611T=	NP_000103.2:p.Leu204=
XM_017009191.2:c.611T=	XP_016864680.1:p.Leu204=
NM_000112.4:c.611T= MANE Select	NP_000103.2:p.Leu204=