Canonical Allele Identifier: CA1590738874
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981647A= , CM000667.2:g.149981647A= GRCh38
NC_000005.9:g.149361210A= , CM000667.1:g.149361210A= GRCh37
NC_000005.8:g.149341403A= NCBI36
NG_007147.2:g.22765A= , LRG_684:g.22765A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.2054A= MANE Select ENSP00000286298.4:p.Gln685=
ENST00000286298.4:c.2054A= ENSP00000286298.4:p.Gln685=
ENST00000503336.1:c.372+3296A= ENSP00000426053.1:n.372+3296A=
NM_000112.3:c.2054A= , LRG_684t1:c.2054A= NP_000103.2:p.Gln685=
XM_017009191.2:c.2054A= XP_016864680.1:p.Gln685=
NM_000112.4:c.2054A= MANE Select NP_000103.2:p.Gln685=