Canonical Allele Identifier: CA1590738985

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981868A= , CM000667.2:g.149981868A=	GRCh38
NC_000005.9:g.149361431A= , CM000667.1:g.149361431A=	GRCh37
NC_000005.8:g.149341624A=	NCBI36
NG_007147.2:g.22986A= , LRG_684:g.22986A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*55A= MANE Select	ENSP00000286298.4:n.*55A=
ENST00000286298.4:c.*55A=	ENSP00000286298.4:n.*55A=
ENST00000503336.1:c.372+3517A=	ENSP00000426053.1:n.372+3517A=
NM_000112.3:c.*55A= , LRG_684t1:c.*55A=	NP_000103.2:n.*55A=
XM_017009191.2:c.*12+43A=	XP_016864680.1:n.*12+43A=
NM_000112.4:c.*55A= MANE Select	NP_000103.2:n.*55A=