Canonical Allele Identifier: CA368749799

Gene: SLC26A5

Linked Data

• MyVariant Identifiers: chr7:g.103015007A>T (hg19) ; chr7:g.103374560A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103374560A>T , CM000669.2:g.103374560A>T	GRCh38
NC_000007.13:g.103015007A>T , CM000669.1:g.103015007A>T	GRCh37
NC_000007.12:g.102802243A>T	NCBI36
NG_023055.1:g.76618T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306312.8:c.2074T>A MANE Select	ENSP00000304783.3:p.Phe692Ile
ENST00000306312.7:c.2074T>A	ENSP00000304783.3:p.Phe692Ile
ENST00000339444.10:c.2041+2248T>A	ENSP00000342396.6:n.2041+2248T>A
ENST00000354356.8:c.2080T>A	ENSP00000346325.5:p.Phe694Ile
ENST00000356767.8:c.972-21634T>A	ENSP00000349210.4:n.972-21634T>A
ENST00000393723.2:c.1984T>A	ENSP00000377324.1:p.Phe662Ile
ENST00000393727.5:c.2080T>A	ENSP00000377328.1:p.Phe694Ile
ENST00000393729.5:c.1963T>A	ENSP00000377330.1:p.Phe655Ile
ENST00000393730.5:c.1978T>A	ENSP00000377331.1:p.Phe660Ile
ENST00000393735.6:c.1514+14448T>A	ENSP00000377336.2:n.1514+14448T>A
ENST00000423416.5:c.*486T>A	ENSP00000389018.1:n.*486T>A
ENST00000432958.6:c.1978T>A	ENSP00000389733.2:p.Phe660Ile
ENST00000445809.5:c.*1057T>A	ENSP00000396833.1:n.*1057T>A
ENST00000454864.5:c.*378T>A	ENSP00000416502.1:n.*378T>A
ENST00000456463.5:c.*1275T>A	ENSP00000395568.1:n.*1275T>A
NM_001167962.1:c.1978T>A	NP_001161434.1:p.Phe660Ile
NM_198999.2:c.2074T>A	NP_945350.1:p.Phe692Ile
NM_206883.2:c.2041+2248T>A	NP_996766.1:n.2041+2248T>A
NM_206884.2:c.1514+14448T>A	NP_996767.1:n.1514+14448T>A
NM_206885.2:c.972-21634T>A	NP_996768.1:n.972-21634T>A
NR_120441.1:n.2090T>A
NR_120442.1:n.1986T>A
NR_120443.1:n.1904T>A
XM_011516170.1:c.2074T>A	XP_011514472.1:p.Phe692Ile
NM_001321787.1:c.1945+2248T>A	NP_001308716.1:n.1945+2248T>A
NR_135801.1:n.2092T>A
NR_135802.1:n.2137+2248T>A
XM_011516170.3:c.2074T>A	XP_011514472.1:p.Phe692Ile
XR_001744725.2:n.2266T>A
XR_001744726.1:n.3023+2248T>A
XR_001744727.2:n.2170T>A
NM_001321787.2:c.1945+2248T>A	NP_001308716.1:n.1945+2248T>A
NM_198999.3:c.2074T>A MANE Select	NP_945350.1:p.Phe692Ile
NM_206883.3:c.2041+2248T>A	NP_996766.1:n.2041+2248T>A
NM_206884.3:c.1514+14448T>A	NP_996767.1:n.1514+14448T>A
NM_206885.3:c.972-21634T>A	NP_996768.1:n.972-21634T>A
NR_135802.2:n.2167+2248T>A
NM_001167962.2:c.1978T>A	NP_001161434.1:p.Phe660Ile
NR_135801.2:n.2122T>A