Canonical Allele Identifier: CA2695208238

Gene: SLC26A4 SLC26A4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107661662_107661677dup , CM000669.2:g.107661662_107661677dup	GRCh38
NC_000007.13:g.107302107_107302122dup , CM000669.1:g.107302107_107302122dup	GRCh37
NC_000007.12:g.107089343_107089358dup	NCBI36
NG_008489.1:g.6028_6043dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.21_36dup (SLC26A4) MANE Select	ENSP00000494017.1:p.Leu13ValfsTer?
ENST00000265715.7:c.21_36dup (SLC26A4)	ENSP00000265715.3:p.Leu13ValfsTer?
ENST00000440056.1:c.21_36dup (SLC26A4)	ENSP00000394760.1:p.Leu13ValfsTer?
NM_000441.1:c.21_36dup (SLC26A4)	NP_000432.1:p.Leu13ValfsTer?
NR_028137.1:n.126_141dup (SLC26A4-AS1)
XM_005250425.1:c.21_36dup (SLC26A4)	XP_005250482.1:p.Leu13ValfsTer?
XM_006716025.2:c.21_36dup (SLC26A4)	XP_006716088.1:p.Leu13ValfsTer?
XM_005250425.2:c.21_36dup (SLC26A4)	XP_005250482.1:p.Leu13ValfsTer?
XM_006716025.3:c.21_36dup (SLC26A4)	XP_006716088.1:p.Leu13ValfsTer?
XM_017012318.1:c.21_36dup (SLC26A4)	XP_016867807.1:p.Leu13ValfsTer?
NM_000441.2:c.21_36dup (SLC26A4) MANE Select	NP_000432.1:p.Leu13ValfsTer?