Canonical Allele Identifier: CA2684353797

Gene: SLC26A5

Linked Data

• gnomAD v4: 7-103420731-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103420731T>C , CM000669.2:g.103420731T>C	GRCh38
NC_000007.13:g.103061178T>C , CM000669.1:g.103061178T>C	GRCh37
NC_000007.12:g.102848414T>C	NCBI36
NG_023055.1:g.30447A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000306312.8:c.292+7A>G MANE Select	ENSP00000304783.3:n.292+7A>G
ENST00000306312.7:c.292+7A>G	ENSP00000304783.3:n.292+7A>G
ENST00000339444.10:c.292+7A>G	ENSP00000342396.6:n.292+7A>G
ENST00000354356.8:c.292+7A>G	ENSP00000346325.5:n.292+7A>G
ENST00000356767.8:c.292+7A>G	ENSP00000349210.4:n.292+7A>G
ENST00000393723.2:c.292+7A>G	ENSP00000377324.1:n.292+7A>G
ENST00000393727.5:c.292+7A>G	ENSP00000377328.1:n.292+7A>G
ENST00000393729.5:c.292+7A>G	ENSP00000377330.1:n.292+7A>G
ENST00000393730.5:c.292+7A>G	ENSP00000377331.1:n.292+7A>G
ENST00000393735.6:c.292+7A>G	ENSP00000377336.2:n.292+7A>G
ENST00000423416.5:c.292+7A>G	ENSP00000389018.1:n.292+7A>G
ENST00000432958.6:c.292+7A>G	ENSP00000389733.2:n.292+7A>G
ENST00000445809.5:c.292+7A>G	ENSP00000396833.1:n.292+7A>G
ENST00000454864.5:c.292+7A>G	ENSP00000416502.1:n.292+7A>G
ENST00000456463.5:c.292+7A>G	ENSP00000395568.1:n.292+7A>G
ENST00000487407.1:n.554+7A>G
NM_001167962.1:c.292+7A>G	NP_001161434.1:n.292+7A>G
NM_198999.2:c.292+7A>G	NP_945350.1:n.292+7A>G
NM_206883.2:c.292+7A>G	NP_996766.1:n.292+7A>G
NM_206884.2:c.292+7A>G	NP_996767.1:n.292+7A>G
NM_206885.2:c.292+7A>G	NP_996768.1:n.292+7A>G
NR_120441.1:n.474+7A>G
NR_120442.1:n.474+7A>G
NR_120443.1:n.474+7A>G
XM_011516170.1:c.292+7A>G	XP_011514472.1:n.292+7A>G
NM_001321787.1:c.292+7A>G	NP_001308716.1:n.292+7A>G
NR_135801.1:n.554+7A>G
NR_135802.1:n.554+7A>G
XM_011516170.3:c.292+7A>G	XP_011514472.1:n.292+7A>G
XR_001744725.2:n.554+7A>G
XR_001744726.1:n.1344+7A>G
XR_001744727.2:n.554+7A>G
XR_002956437.1:n.554+7A>G
NM_001321787.2:c.292+7A>G	NP_001308716.1:n.292+7A>G
NM_198999.3:c.292+7A>G MANE Select	NP_945350.1:n.292+7A>G
NM_206883.3:c.292+7A>G	NP_996766.1:n.292+7A>G
NM_206884.3:c.292+7A>G	NP_996767.1:n.292+7A>G
NM_206885.3:c.292+7A>G	NP_996768.1:n.292+7A>G
NR_135802.2:n.584+7A>G
NM_001167962.2:c.292+7A>G	NP_001161434.1:n.292+7A>G
NR_135801.2:n.584+7A>G