Canonical Allele Identifier: CA361704944
Gene: SLC26A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978068A>T , CM000667.2:g.149978068A>T GRCh38
NC_000005.9:g.149357631A>T , CM000667.1:g.149357631A>T GRCh37
NC_000005.8:g.149337824A>T NCBI36
NG_007147.2:g.19186A>T , LRG_684:g.19186A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.648A>T
ENST00000286298.5:c.416A>T MANE Select ENSP00000286298.4:p.Tyr139Phe
ENST00000286298.4:c.416A>T ENSP00000286298.4:p.Tyr139Phe
ENST00000503336.1:c.89A>T ENSP00000426053.1:p.Tyr30Phe
NM_000112.3:c.416A>T , LRG_684t1:c.416A>T NP_000103.2:p.Tyr139Phe
XM_017009191.2:c.416A>T XP_016864680.1:p.Tyr139Phe
NM_000112.4:c.416A>T MANE Select NP_000103.2:p.Tyr139Phe