Canonical Allele Identifier: CA447401951

Gene: SLC26A2

Linked Data

• MyVariant Identifiers: chr5:g.149357629C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978066C>T , CM000667.2:g.149978066C>T	GRCh38
NC_000005.9:g.149357629C>T , CM000667.1:g.149357629C>T	GRCh37
NC_000005.8:g.149337822C>T	NCBI36
NG_007147.2:g.19184C>T , LRG_684:g.19184C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.646C>T
ENST00000286298.5:c.414C>T MANE Select	ENSP00000286298.4:p.Val138=
ENST00000286298.4:c.414C>T	ENSP00000286298.4:p.Val138=
ENST00000503336.1:c.87C>T	ENSP00000426053.1:p.Val29=
NM_000112.3:c.414C>T , LRG_684t1:c.414C>T	NP_000103.2:p.Val138=
XM_017009191.2:c.414C>T	XP_016864680.1:p.Val138=
NM_000112.4:c.414C>T MANE Select	NP_000103.2:p.Val138=