Canonical Allele Identifier: CA1590737277

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149977766C= , CM000667.2:g.149977766C=	GRCh38
NC_000005.9:g.149357329C= , CM000667.1:g.149357329C=	GRCh37
NC_000005.8:g.149337522C=	NCBI36
NG_007147.2:g.18884C= , LRG_684:g.18884C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000690410.1:n.346C=
ENST00000286298.5:c.114C= MANE Select	ENSP00000286298.4:p.Asp38=
ENST00000286298.4:c.114C=	ENSP00000286298.4:p.Asp38=
NM_000112.3:c.114C= , LRG_684t1:c.114C=	NP_000103.2:p.Asp38=
XM_017009191.2:c.114C=	XP_016864680.1:p.Asp38=
NM_000112.4:c.114C= MANE Select	NP_000103.2:p.Asp38=