Canonical Allele Identifier: CA1730703549

Gene: SLC26A5

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103374479G= , CM000669.2:g.103374479G=	GRCh38
NC_000007.13:g.103014926G= , CM000669.1:g.103014926G=	GRCh37
NC_000007.12:g.102802162G=	NCBI36
NG_023055.1:g.76699C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306312.8:c.2155C= MANE Select	ENSP00000304783.3:p.Leu719=
ENST00000306312.7:c.2155C=	ENSP00000304783.3:p.Leu719=
ENST00000339444.10:c.2041+2329C=	ENSP00000342396.6:n.2041+2329C=
ENST00000354356.8:c.2161C=	ENSP00000346325.5:p.Leu721=
ENST00000356767.8:c.972-21553C=	ENSP00000349210.4:n.972-21553C=
ENST00000393723.2:c.2065C=	ENSP00000377324.1:p.Leu689=
ENST00000393727.5:c.2161C=	ENSP00000377328.1:p.Leu721=
ENST00000393729.5:c.2044C=	ENSP00000377330.1:p.Leu682=
ENST00000393730.5:c.2059C=	ENSP00000377331.1:p.Leu687=
ENST00000393735.6:c.1514+14529C=	ENSP00000377336.2:n.1514+14529C=
ENST00000423416.5:c.*567C=	ENSP00000389018.1:n.*567C=
ENST00000432958.6:c.2059C=	ENSP00000389733.2:p.Leu687=
ENST00000445809.5:c.*1138C=	ENSP00000396833.1:n.*1138C=
ENST00000454864.5:c.*459C=	ENSP00000416502.1:n.*459C=
ENST00000456463.5:c.*1356C=	ENSP00000395568.1:n.*1356C=
NM_001167962.1:c.2059C=	NP_001161434.1:p.Leu687=
NM_198999.2:c.2155C=	NP_945350.1:p.Leu719=
NM_206883.2:c.2041+2329C=	NP_996766.1:n.2041+2329C=
NM_206884.2:c.1514+14529C=	NP_996767.1:n.1514+14529C=
NM_206885.2:c.972-21553C=	NP_996768.1:n.972-21553C=
NR_120441.1:n.2171C=
NR_120442.1:n.2067C=
NR_120443.1:n.1985C=
XM_011516170.1:c.2155C=	XP_011514472.1:p.Leu719=
NM_001321787.1:c.1945+2329C=	NP_001308716.1:n.1945+2329C=
NR_135801.1:n.2173C=
NR_135802.1:n.2137+2329C=
XM_011516170.3:c.2155C=	XP_011514472.1:p.Leu719=
XR_001744725.2:n.2347C=
XR_001744726.1:n.3023+2329C=
XR_001744727.2:n.2251C=
NM_001321787.2:c.1945+2329C=	NP_001308716.1:n.1945+2329C=
NM_198999.3:c.2155C= MANE Select	NP_945350.1:p.Leu719=
NM_206883.3:c.2041+2329C=	NP_996766.1:n.2041+2329C=
NM_206884.3:c.1514+14529C=	NP_996767.1:n.1514+14529C=
NM_206885.3:c.972-21553C=	NP_996768.1:n.972-21553C=
NR_135802.2:n.2167+2329C=
NM_001167962.2:c.2059C=	NP_001161434.1:p.Leu687=
NR_135801.2:n.2203C=