Canonical Allele Identifier: CA361704915

Gene: SLC26A2

Linked Data

• gnomAD v4: 5-149978055-C-T
• MyVariant Identifiers: chr5:g.149357618C>T (hg19) ; chr5:g.149978055C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978055C>T , CM000667.2:g.149978055C>T	GRCh38
NC_000005.9:g.149357618C>T , CM000667.1:g.149357618C>T	GRCh37
NC_000005.8:g.149337811C>T	NCBI36
NG_007147.2:g.19173C>T , LRG_684:g.19173C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.635C>T
ENST00000286298.5:c.403C>T MANE Select	ENSP00000286298.4:p.Gln135Ter
ENST00000286298.4:c.403C>T	ENSP00000286298.4:p.Gln135Ter
ENST00000503336.1:c.76C>T	ENSP00000426053.1:p.Gln26Ter
NM_000112.3:c.403C>T , LRG_684t1:c.403C>T	NP_000103.2:p.Gln135Ter
XM_017009191.2:c.403C>T	XP_016864680.1:p.Gln135Ter
NM_000112.4:c.403C>T MANE Select	NP_000103.2:p.Gln135Ter