Canonical Allele Identifier: CA1590738542
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149980840A= , CM000667.2:g.149980840A= GRCh38
NC_000005.9:g.149360403A= , CM000667.1:g.149360403A= GRCh37
NC_000005.8:g.149340596A= NCBI36
NG_007147.2:g.21958A= , LRG_684:g.21958A=

Transcript Alleles

HGVS Amino-acid change
ENST00000286298.5:c.1247A= MANE Select ENSP00000286298.4:p.Gln416=
ENST00000286298.4:c.1247A= ENSP00000286298.4:p.Gln416=
ENST00000503336.1:c.372+2489A= ENSP00000426053.1:n.372+2489A=
NM_000112.3:c.1247A= , LRG_684t1:c.1247A= NP_000103.2:p.Gln416=
XM_017009191.2:c.1247A= XP_016864680.1:p.Gln416=
NM_000112.4:c.1247A= MANE Select NP_000103.2:p.Gln416=