Canonical Allele Identifier: CA1590737414

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978121T= , CM000667.2:g.149978121T=	GRCh38
NC_000005.9:g.149357684T= , CM000667.1:g.149357684T=	GRCh37
NC_000005.8:g.149337877T=	NCBI36
NG_007147.2:g.19239T= , LRG_684:g.19239T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.701T=
ENST00000286298.5:c.469T= MANE Select	ENSP00000286298.4:p.Ser157=
ENST00000286298.4:c.469T=	ENSP00000286298.4:p.Ser157=
ENST00000503336.1:c.142T=	ENSP00000426053.1:p.Ser48=
NM_000112.3:c.469T= , LRG_684t1:c.469T=	NP_000103.2:p.Ser157=
XM_017009191.2:c.469T=	XP_016864680.1:p.Ser157=
NM_000112.4:c.469T= MANE Select	NP_000103.2:p.Ser157=