Canonical Allele Identifier: CA913111815

Gene: SLC26A4

Linked Data

• MyVariant Identifiers: chr7:g.107312626_107312627del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107672184_107672185del , CM000669.2:g.107672184_107672185del	GRCh38
NC_000007.13:g.107312629_107312630del , CM000669.1:g.107312629_107312630del	GRCh37
NC_000007.12:g.107099865_107099866del	NCBI36
NG_008489.1:g.16550_16551del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.351_352del MANE Select	ENSP00000494017.1:p.Tyr118LeufsTer?
ENST00000265715.7:c.351_352del	ENSP00000265715.3:p.Tyr118LeufsTer?
ENST00000440056.1:c.351_352del	ENSP00000394760.1:p.Tyr118LeufsTer?
NM_000441.1:c.351_352del	NP_000432.1:p.Tyr118LeufsTer?
XM_005250425.1:c.351_352del	XP_005250482.1:p.Tyr118LeufsTer?
XM_006716025.2:c.351_352del	XP_006716088.1:p.Tyr118LeufsTer?
XM_005250425.2:c.351_352del	XP_005250482.1:p.Tyr118LeufsTer?
XM_006716025.3:c.351_352del	XP_006716088.1:p.Tyr118LeufsTer?
XM_017012318.1:c.351_352del	XP_016867807.1:p.Tyr118LeufsTer?
NM_000441.2:c.351_352del MANE Select	NP_000432.1:p.Tyr118LeufsTer?