Canonical Allele Identifier: CA831174114

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1339858065
• MyVariant Identifiers: chr7:g.107350224_107350225insAAAT (hg19) ; chr7:g.107709779_107709780insAAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107709791_107709794dup , CM000669.2:g.107709791_107709794dup	GRCh38
NC_000007.13:g.107350236_107350239dup , CM000669.1:g.107350236_107350239dup	GRCh37
NC_000007.12:g.107137472_107137475dup	NCBI36
NG_008489.1:g.54157_54160dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2090-263_2090-260dup MANE Select	ENSP00000494017.1:n.2090-263_2090-260dup
ENST00000644846.1:c.746-263_746-260dup
ENST00000265715.7:c.2090-263_2090-260dup	ENSP00000265715.3:n.2090-263_2090-260dup
ENST00000492030.2:n.377-364_377-361dup
NM_000441.1:c.2090-263_2090-260dup	NP_000432.1:n.2090-263_2090-260dup
XM_005250425.1:c.2090-263_2090-260dup	XP_005250482.1:n.2090-263_2090-260dup
XM_005250425.2:c.2090-263_2090-260dup	XP_005250482.1:n.2090-263_2090-260dup
XM_017012318.1:c.2012-263_2012-260dup	XP_016867807.1:n.2012-263_2012-260dup
NM_000441.2:c.2090-263_2090-260dup MANE Select	NP_000432.1:n.2090-263_2090-260dup