Canonical Allele Identifier: CA1590737533
Gene: SLC26A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978401A= , CM000667.2:g.149978401A= GRCh38
NC_000005.9:g.149357964A= , CM000667.1:g.149357964A= GRCh37
NC_000005.8:g.149338157A= NCBI36
NG_007147.2:g.19519A= , LRG_684:g.19519A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.981A=
ENST00000286298.5:c.699+50A= MANE Select ENSP00000286298.4:n.699+50A=
ENST00000286298.4:c.699+50A= ENSP00000286298.4:n.699+50A=
ENST00000503336.1:c.372+50A= ENSP00000426053.1:n.372+50A=
NM_000112.3:c.699+50A= , LRG_684t1:c.699+50A= NP_000103.2:n.699+50A=
XM_017009191.2:c.699+50A= XP_016864680.1:n.699+50A=
NM_000112.4:c.699+50A= MANE Select NP_000103.2:n.699+50A=
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