Canonical Allele Identifier: CA1590738519

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149980779A= , CM000667.2:g.149980779A=	GRCh38
NC_000005.9:g.149360342A= , CM000667.1:g.149360342A=	GRCh37
NC_000005.8:g.149340535A=	NCBI36
NG_007147.2:g.21897A= , LRG_684:g.21897A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000286298.5:c.1186A= MANE Select	ENSP00000286298.4:p.Ile396=
ENST00000286298.4:c.1186A=	ENSP00000286298.4:p.Ile396=
ENST00000503336.1:c.372+2428A=	ENSP00000426053.1:n.372+2428A=
NM_000112.3:c.1186A= , LRG_684t1:c.1186A=	NP_000103.2:p.Ile396=
XM_017009191.2:c.1186A=	XP_016864680.1:p.Ile396=
NM_000112.4:c.1186A= MANE Select	NP_000103.2:p.Ile396=