Canonical Allele Identifier: CA1732758407

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701131_107701133delinsAAG , CM000669.2:g.107701131_107701133delinsAAG	GRCh38
NC_000007.13:g.107341576_107341578delinsAAG , CM000669.1:g.107341576_107341578delinsAAG	GRCh37
NC_000007.12:g.107128812_107128814delinsAAG	NCBI36
NG_008489.1:g.45497_45499delinsAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1738_1740delinsAAG MANE Select	ENSP00000494017.1:p.Lys580=
ENST00000644846.1:c.449_451delinsAAG
ENST00000265715.7:c.1738_1740delinsAAG	ENSP00000265715.3:p.Lys580=
ENST00000480841.5:n.587_589delinsAAG
ENST00000492030.2:n.91-696_91-694delinsAAG
NM_000441.1:c.1738_1740delinsAAG	NP_000432.1:p.Lys580=
XM_005250425.1:c.1738_1740delinsAAG	XP_005250482.1:p.Lys580=
XM_005250425.2:c.1738_1740delinsAAG	XP_005250482.1:p.Lys580=
XM_017012318.1:c.1660_1662delinsAAG	XP_016867807.1:p.Lys554=
NM_000441.2:c.1738_1740delinsAAG MANE Select	NP_000432.1:p.Lys580=