Canonical Allele Identifier: CA1590737374

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978039T= , CM000667.2:g.149978039T=	GRCh38
NC_000005.9:g.149357602T= , CM000667.1:g.149357602T=	GRCh37
NC_000005.8:g.149337795T=	NCBI36
NG_007147.2:g.19157T= , LRG_684:g.19157T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.619T=
ENST00000286298.5:c.387T= MANE Select	ENSP00000286298.4:p.Tyr129=
ENST00000286298.4:c.387T=	ENSP00000286298.4:p.Tyr129=
ENST00000503336.1:c.60T=	ENSP00000426053.1:p.Tyr20=
NM_000112.3:c.387T= , LRG_684t1:c.387T=	NP_000103.2:p.Tyr129=
XM_017009191.2:c.387T=	XP_016864680.1:p.Tyr129=
NM_000112.4:c.387T= MANE Select	NP_000103.2:p.Tyr129=