Canonical Allele Identifier: CA368749707

Gene: SLC26A5

Linked Data

• MyVariant Identifiers: chr7:g.103014967C>G (hg19) ; chr7:g.103374520C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103374520C>G , CM000669.2:g.103374520C>G	GRCh38
NC_000007.13:g.103014967C>G , CM000669.1:g.103014967C>G	GRCh37
NC_000007.12:g.102802203C>G	NCBI36
NG_023055.1:g.76658G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306312.8:c.2114G>C MANE Select	ENSP00000304783.3:p.Ser705Thr
ENST00000306312.7:c.2114G>C	ENSP00000304783.3:p.Ser705Thr
ENST00000339444.10:c.2041+2288G>C	ENSP00000342396.6:n.2041+2288G>C
ENST00000354356.8:c.2120G>C	ENSP00000346325.5:p.Ser707Thr
ENST00000356767.8:c.972-21594G>C	ENSP00000349210.4:n.972-21594G>C
ENST00000393723.2:c.2024G>C	ENSP00000377324.1:p.Ser675Thr
ENST00000393727.5:c.2120G>C	ENSP00000377328.1:p.Ser707Thr
ENST00000393729.5:c.2003G>C	ENSP00000377330.1:p.Ser668Thr
ENST00000393730.5:c.2018G>C	ENSP00000377331.1:p.Ser673Thr
ENST00000393735.6:c.1514+14488G>C	ENSP00000377336.2:n.1514+14488G>C
ENST00000423416.5:c.*526G>C	ENSP00000389018.1:n.*526G>C
ENST00000432958.6:c.2018G>C	ENSP00000389733.2:p.Ser673Thr
ENST00000445809.5:c.*1097G>C	ENSP00000396833.1:n.*1097G>C
ENST00000454864.5:c.*418G>C	ENSP00000416502.1:n.*418G>C
ENST00000456463.5:c.*1315G>C	ENSP00000395568.1:n.*1315G>C
NM_001167962.1:c.2018G>C	NP_001161434.1:p.Ser673Thr
NM_198999.2:c.2114G>C	NP_945350.1:p.Ser705Thr
NM_206883.2:c.2041+2288G>C	NP_996766.1:n.2041+2288G>C
NM_206884.2:c.1514+14488G>C	NP_996767.1:n.1514+14488G>C
NM_206885.2:c.972-21594G>C	NP_996768.1:n.972-21594G>C
NR_120441.1:n.2130G>C
NR_120442.1:n.2026G>C
NR_120443.1:n.1944G>C
XM_011516170.1:c.2114G>C	XP_011514472.1:p.Ser705Thr
NM_001321787.1:c.1945+2288G>C	NP_001308716.1:n.1945+2288G>C
NR_135801.1:n.2132G>C
NR_135802.1:n.2137+2288G>C
XM_011516170.3:c.2114G>C	XP_011514472.1:p.Ser705Thr
XR_001744725.2:n.2306G>C
XR_001744726.1:n.3023+2288G>C
XR_001744727.2:n.2210G>C
NM_001321787.2:c.1945+2288G>C	NP_001308716.1:n.1945+2288G>C
NM_198999.3:c.2114G>C MANE Select	NP_945350.1:p.Ser705Thr
NM_206883.3:c.2041+2288G>C	NP_996766.1:n.2041+2288G>C
NM_206884.3:c.1514+14488G>C	NP_996767.1:n.1514+14488G>C
NM_206885.3:c.972-21594G>C	NP_996768.1:n.972-21594G>C
NR_135802.2:n.2167+2288G>C
NM_001167962.2:c.2018G>C	NP_001161434.1:p.Ser673Thr
NR_135801.2:n.2162G>C