Canonical Allele Identifier: CA1139667644

Gene: GJB1

Linked Data

• ClinVar Variation Id: 943937
• ClinVar RCV Id: RCV001214227
• dbSNP Id: rs2092542575

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71223818_71223819dup , CM000685.2:g.71223818_71223819dup	GRCh38
NC_000023.10:g.70443668_70443669dup , CM000685.1:g.70443668_70443669dup	GRCh37
NC_000023.9:g.70360393_70360394dup	NCBI36
NG_008357.1:g.13607_13608dup , LRG_245:g.13607_13608dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361726.7:c.111_112dup MANE Select	ENSP00000354900.6:p.Val38GlyfsTer?
ENST00000374029.2:c.111_112dup	ENSP00000363141.1:p.Val38GlyfsTer?
ENST00000447581.2:c.111_112dup	ENSP00000407223.2:p.Val38GlyfsTer?
ENST00000645009.2:c.111_112dup	ENSP00000494142.2:p.Val38GlyfsTer?
ENST00000646835.1:c.111_112dup	ENSP00000494596.1:p.Val38GlyfsTer?
ENST00000647424.1:c.111_112dup	ENSP00000495960.1:p.Val38GlyfsTer?
ENST00000674549.1:c.111_112dup	ENSP00000502766.1:p.Val38GlyfsTer?
ENST00000674844.1:c.111_112dup	ENSP00000502556.1:p.Val38GlyfsTer?
ENST00000675209.1:c.111_112dup	ENSP00000501813.1:p.Val38GlyfsTer?
ENST00000675368.1:c.111_112dup	ENSP00000501757.1:p.Val38GlyfsTer?
ENST00000675609.1:c.111_112dup	ENSP00000501571.1:p.Val38GlyfsTer?
ENST00000361726.6:c.111_112dup	ENSP00000354900.6:p.Val38GlyfsTer?
ENST00000374022.3:c.111_112dup	ENSP00000363134.3:p.Val38GlyfsTer?
ENST00000374029.1:c.111_112dup	ENSP00000363141.1:p.Val38GlyfsTer?
ENST00000447581.1:c.111_112dup	ENSP00000407223.1:p.Val38GlyfsTer?
NM_000166.5:c.111_112dup	NP_000157.1:p.Val38GlyfsTer?
NM_001097642.2:c.111_112dup , LRG_245t1:c.111_112dup	NP_001091111.1:p.Val38GlyfsTer?
XM_011530907.1:c.111_112dup	XP_011529209.1:p.Val38GlyfsTer?
XM_011530907.2:c.111_112dup	XP_011529209.1:p.Val38GlyfsTer?
NM_000166.6:c.111_112dup MANE Select	NP_000157.1:p.Val38GlyfsTer?
NM_001097642.3:c.111_112dup	NP_001091111.1:p.Val38GlyfsTer?