Canonical Allele Identifier: CA1732750917
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107709813_107709818delinsTTAGTA , CM000669.2:g.107709813_107709818delinsTTAGTA GRCh38
NC_000007.13:g.107350258_107350263delinsTTAGTA , CM000669.1:g.107350258_107350263delinsTTAGTA GRCh37
NC_000007.12:g.107137494_107137499delinsTTAGTA NCBI36
NG_008489.1:g.54179_54184delinsTTAGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2090-241_2090-236delinsTTAGTA MANE Select ENSP00000494017.1:n.2090-241_2090-236delinsTTAGTA
ENST00000644846.1:c.746-241_746-236delinsTTAGTA
ENST00000265715.7:c.2090-241_2090-236delinsTTAGTA ENSP00000265715.3:n.2090-241_2090-236delinsTTAGTA
ENST00000492030.2:n.377-342_377-337delinsTTAGTA
NM_000441.1:c.2090-241_2090-236delinsTTAGTA NP_000432.1:n.2090-241_2090-236delinsTTAGTA
XM_005250425.1:c.2090-241_2090-236delinsTTAGTA XP_005250482.1:n.2090-241_2090-236delinsTTAGTA
XM_005250425.2:c.2090-241_2090-236delinsTTAGTA XP_005250482.1:n.2090-241_2090-236delinsTTAGTA
XM_017012318.1:c.2012-241_2012-236delinsTTAGTA XP_016867807.1:n.2012-241_2012-236delinsTTAGTA
NM_000441.2:c.2090-241_2090-236delinsTTAGTA MANE Select NP_000432.1:n.2090-241_2090-236delinsTTAGTA