Canonical Allele Identifier: CA368749779

Gene: SLC26A5

Linked Data

• MyVariant Identifiers: chr7:g.103014999T>G (hg19) ; chr7:g.103374552T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103374552T>G , CM000669.2:g.103374552T>G	GRCh38
NC_000007.13:g.103014999T>G , CM000669.1:g.103014999T>G	GRCh37
NC_000007.12:g.102802235T>G	NCBI36
NG_023055.1:g.76626A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306312.8:c.2082A>C MANE Select	ENSP00000304783.3:p.Glu694Asp
ENST00000306312.7:c.2082A>C	ENSP00000304783.3:p.Glu694Asp
ENST00000339444.10:c.2041+2256A>C	ENSP00000342396.6:n.2041+2256A>C
ENST00000354356.8:c.2088A>C	ENSP00000346325.5:p.Glu696Asp
ENST00000356767.8:c.972-21626A>C	ENSP00000349210.4:n.972-21626A>C
ENST00000393723.2:c.1992A>C	ENSP00000377324.1:p.Glu664Asp
ENST00000393727.5:c.2088A>C	ENSP00000377328.1:p.Glu696Asp
ENST00000393729.5:c.1971A>C	ENSP00000377330.1:p.Glu657Asp
ENST00000393730.5:c.1986A>C	ENSP00000377331.1:p.Glu662Asp
ENST00000393735.6:c.1514+14456A>C	ENSP00000377336.2:n.1514+14456A>C
ENST00000423416.5:c.*494A>C	ENSP00000389018.1:n.*494A>C
ENST00000432958.6:c.1986A>C	ENSP00000389733.2:p.Glu662Asp
ENST00000445809.5:c.*1065A>C	ENSP00000396833.1:n.*1065A>C
ENST00000454864.5:c.*386A>C	ENSP00000416502.1:n.*386A>C
ENST00000456463.5:c.*1283A>C	ENSP00000395568.1:n.*1283A>C
NM_001167962.1:c.1986A>C	NP_001161434.1:p.Glu662Asp
NM_198999.2:c.2082A>C	NP_945350.1:p.Glu694Asp
NM_206883.2:c.2041+2256A>C	NP_996766.1:n.2041+2256A>C
NM_206884.2:c.1514+14456A>C	NP_996767.1:n.1514+14456A>C
NM_206885.2:c.972-21626A>C	NP_996768.1:n.972-21626A>C
NR_120441.1:n.2098A>C
NR_120442.1:n.1994A>C
NR_120443.1:n.1912A>C
XM_011516170.1:c.2082A>C	XP_011514472.1:p.Glu694Asp
NM_001321787.1:c.1945+2256A>C	NP_001308716.1:n.1945+2256A>C
NR_135801.1:n.2100A>C
NR_135802.1:n.2137+2256A>C
XM_011516170.3:c.2082A>C	XP_011514472.1:p.Glu694Asp
XR_001744725.2:n.2274A>C
XR_001744726.1:n.3023+2256A>C
XR_001744727.2:n.2178A>C
NM_001321787.2:c.1945+2256A>C	NP_001308716.1:n.1945+2256A>C
NM_198999.3:c.2082A>C MANE Select	NP_945350.1:p.Glu694Asp
NM_206883.3:c.2041+2256A>C	NP_996766.1:n.2041+2256A>C
NM_206884.3:c.1514+14456A>C	NP_996767.1:n.1514+14456A>C
NM_206885.3:c.972-21626A>C	NP_996768.1:n.972-21626A>C
NR_135802.2:n.2167+2256A>C
NM_001167962.2:c.1986A>C	NP_001161434.1:p.Glu662Asp
NR_135801.2:n.2130A>C