Canonical Allele Identifier: CA1590738765
Gene: SLC26A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981407_149981408delinsAC , CM000667.2:g.149981407_149981408delinsAC GRCh38
NC_000005.9:g.149360970_149360971delinsAC , CM000667.1:g.149360970_149360971delinsAC GRCh37
NC_000005.8:g.149341163_149341164delinsAC NCBI36
NG_007147.2:g.22525_22526delinsAC , LRG_684:g.22525_22526delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.1814_1815delinsAC MANE Select ENSP00000286298.4:p.Asn605=
ENST00000286298.4:c.1814_1815delinsAC ENSP00000286298.4:p.Asn605=
ENST00000503336.1:c.372+3056_372+3057delinsAC ENSP00000426053.1:n.372+3056_372+3057delinsAC
NM_000112.3:c.1814_1815delinsAC , LRG_684t1:c.1814_1815delinsAC NP_000103.2:p.Asn605=
XM_017009191.2:c.1814_1815delinsAC XP_016864680.1:p.Asn605=
NM_000112.4:c.1814_1815delinsAC MANE Select NP_000103.2:p.Asn605=
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