Canonical Allele Identifier: CA1590737434
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978164T= , CM000667.2:g.149978164T= GRCh38
NC_000005.9:g.149357727T= , CM000667.1:g.149357727T= GRCh37
NC_000005.8:g.149337920T= NCBI36
NG_007147.2:g.19282T= , LRG_684:g.19282T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.744T=
ENST00000286298.5:c.512T= MANE Select ENSP00000286298.4:p.Met171=
ENST00000286298.4:c.512T= ENSP00000286298.4:p.Met171=
ENST00000503336.1:c.185T= ENSP00000426053.1:p.Met62=
NM_000112.3:c.512T= , LRG_684t1:c.512T= NP_000103.2:p.Met171=
XM_017009191.2:c.512T= XP_016864680.1:p.Met171=
NM_000112.4:c.512T= MANE Select NP_000103.2:p.Met171=