Canonical Allele Identifier: CA2535362013

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107709995_107709996insTA , CM000669.2:g.107709995_107709996insTA	GRCh38
NC_000007.13:g.107350440_107350441insTA , CM000669.1:g.107350440_107350441insTA	GRCh37
NC_000007.12:g.107137676_107137677insTA	NCBI36
NG_008489.1:g.54361_54362insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2090-59_2090-58insTA MANE Select	ENSP00000494017.1:n.2090-59_2090-58insTA
ENST00000644846.1:c.746-59_746-58insTA
ENST00000265715.7:c.2090-59_2090-58insTA	ENSP00000265715.3:n.2090-59_2090-58insTA
ENST00000492030.2:n.377-160_377-159insTA
NM_000441.1:c.2090-59_2090-58insTA	NP_000432.1:n.2090-59_2090-58insTA
XM_005250425.1:c.2090-59_2090-58insTA	XP_005250482.1:n.2090-59_2090-58insTA
XM_005250425.2:c.2090-59_2090-58insTA	XP_005250482.1:n.2090-59_2090-58insTA
XM_017012318.1:c.2012-59_2012-58insTA	XP_016867807.1:n.2012-59_2012-58insTA
NM_000441.2:c.2090-59_2090-58insTA MANE Select	NP_000432.1:n.2090-59_2090-58insTA