Canonical Allele Identifier: CA1732751005

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107709910_107709916delinsCACTTGA , CM000669.2:g.107709910_107709916delinsCACTTGA	GRCh38
NC_000007.13:g.107350355_107350361delinsCACTTGA , CM000669.1:g.107350355_107350361delinsCACTTGA	GRCh37
NC_000007.12:g.107137591_107137597delinsCACTTGA	NCBI36
NG_008489.1:g.54276_54282delinsCACTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2090-144_2090-138delinsCACTTGA MANE Select	ENSP00000494017.1:n.2090-144_2090-138delinsCACTTGA
ENST00000644846.1:c.746-144_746-138delinsCACTTGA
ENST00000265715.7:c.2090-144_2090-138delinsCACTTGA	ENSP00000265715.3:n.2090-144_2090-138delinsCACTTGA
ENST00000492030.2:n.377-245_377-239delinsCACTTGA
NM_000441.1:c.2090-144_2090-138delinsCACTTGA	NP_000432.1:n.2090-144_2090-138delinsCACTTGA
XM_005250425.1:c.2090-144_2090-138delinsCACTTGA	XP_005250482.1:n.2090-144_2090-138delinsCACTTGA
XM_005250425.2:c.2090-144_2090-138delinsCACTTGA	XP_005250482.1:n.2090-144_2090-138delinsCACTTGA
XM_017012318.1:c.2012-144_2012-138delinsCACTTGA	XP_016867807.1:n.2012-144_2012-138delinsCACTTGA
NM_000441.2:c.2090-144_2090-138delinsCACTTGA MANE Select	NP_000432.1:n.2090-144_2090-138delinsCACTTGA