Canonical Allele Identifier: CA361705390

Gene: SLC26A2

Linked Data

• MyVariant Identifiers: chr5:g.149357841A>T (hg19) ; chr5:g.149978278A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978278A>T , CM000667.2:g.149978278A>T	GRCh38
NC_000005.9:g.149357841A>T , CM000667.1:g.149357841A>T	GRCh37
NC_000005.8:g.149338034A>T	NCBI36
NG_007147.2:g.19396A>T , LRG_684:g.19396A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.858A>T
ENST00000286298.5:c.626A>T MANE Select	ENSP00000286298.4:p.Asp209Val
ENST00000286298.4:c.626A>T	ENSP00000286298.4:p.Asp209Val
ENST00000503336.1:c.299A>T	ENSP00000426053.1:p.Asp100Val
NM_000112.3:c.626A>T , LRG_684t1:c.626A>T	NP_000103.2:p.Asp209Val
XM_017009191.2:c.626A>T	XP_016864680.1:p.Asp209Val
NM_000112.4:c.626A>T MANE Select	NP_000103.2:p.Asp209Val