Canonical Allele Identifier: CA1590739022

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981958T= , CM000667.2:g.149981958T=	GRCh38
NC_000005.9:g.149361521T= , CM000667.1:g.149361521T=	GRCh37
NC_000005.8:g.149341714T=	NCBI36
NG_007147.2:g.23076T= , LRG_684:g.23076T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*145T= MANE Select	ENSP00000286298.4:n.*145T=
ENST00000286298.4:c.*145T=	ENSP00000286298.4:n.*145T=
ENST00000503336.1:c.372+3607T=	ENSP00000426053.1:n.372+3607T=
NM_000112.3:c.*145T= , LRG_684t1:c.*145T=	NP_000103.2:n.*145T=
XM_017009191.2:c.*42T=	XP_016864680.1:n.*42T=
NM_000112.4:c.*145T= MANE Select	NP_000103.2:n.*145T=