Canonical Allele Identifier: CA1590737321

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149977868A= , CM000667.2:g.149977868A=	GRCh38
NC_000005.9:g.149357431A= , CM000667.1:g.149357431A=	GRCh37
NC_000005.8:g.149337624A=	NCBI36
NG_007147.2:g.18986A= , LRG_684:g.18986A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000690410.1:n.448A=
ENST00000286298.5:c.216A= MANE Select	ENSP00000286298.4:p.Lys72=
ENST00000286298.4:c.216A=	ENSP00000286298.4:p.Lys72=
NM_000112.3:c.216A= , LRG_684t1:c.216A=	NP_000103.2:p.Lys72=
XM_017009191.2:c.216A=	XP_016864680.1:p.Lys72=
NM_000112.4:c.216A= MANE Select	NP_000103.2:p.Lys72=