Canonical Allele Identifier: CA1590738425

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149980571A= , CM000667.2:g.149980571A=	GRCh38
NC_000005.9:g.149360134A= , CM000667.1:g.149360134A=	GRCh37
NC_000005.8:g.149340327A=	NCBI36
NG_007147.2:g.21689A= , LRG_684:g.21689A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.978A= MANE Select	ENSP00000286298.4:p.Lys326=
ENST00000286298.4:c.978A=	ENSP00000286298.4:p.Lys326=
ENST00000503336.1:c.372+2220A=	ENSP00000426053.1:n.372+2220A=
NM_000112.3:c.978A= , LRG_684t1:c.978A=	NP_000103.2:p.Lys326=
XM_017009191.2:c.978A=	XP_016864680.1:p.Lys326=
NM_000112.4:c.978A= MANE Select	NP_000103.2:p.Lys326=