Canonical Allele Identifier: CA2077159895

Gene: GJB6

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.20223123C= , CM000675.2:g.20223123C=	GRCh38
NC_000013.10:g.20797262C= , CM000675.1:g.20797262C=	GRCh37
NC_000013.9:g.19695262C=	NCBI36
NG_008323.1:g.14273G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241124.11:c.358G=	ENSP00000241124.6:p.Asp120=
ENST00000400066.8:c.358G=	ENSP00000382939.3:p.Asp120=
ENST00000636852.1:c.358G=	ENSP00000489698.1:p.Asp120=
ENST00000643121.1:c.358G=	ENSP00000494468.1:p.Asp120=
ENST00000643211.1:c.358G=	ENSP00000495841.1:p.Asp120=
ENST00000644283.1:c.358G=	ENSP00000495320.1:p.Asp120=
ENST00000644667.1:c.358G=	ENSP00000493621.1:p.Asp120=
ENST00000647029.1:c.358G= MANE Select	ENSP00000493834.1:p.Asp120=
ENST00000647243.1:c.358G=	ENSP00000494733.1:p.Asp120=
ENST00000241124.10:c.358G=	ENSP00000241124.6:p.Asp120=
ENST00000356192.6:c.358G=	ENSP00000348521.6:p.Asp120=
ENST00000400065.7:c.358G=	ENSP00000382938.3:p.Asp120=
ENST00000400066.7:c.358G=	ENSP00000382939.3:p.Asp120=
NM_001110219.2:c.358G=	NP_001103689.1:p.Asp120=
NM_001110220.2:c.358G=	NP_001103690.1:p.Asp120=
NM_001110221.2:c.358G=	NP_001103691.1:p.Asp120=
NM_006783.4:c.358G=	NP_006774.2:p.Asp120=
NM_001110219.3:c.358G= MANE Select	NP_001103689.1:p.Asp120=
NM_001370090.1:c.358G=	NP_001357019.1:p.Asp120=
NM_001370091.1:c.358G=	NP_001357020.1:p.Asp120=
NM_001370092.1:c.358G=	NP_001357021.1:p.Asp120=
NM_001110220.3:c.358G=	NP_001103690.1:p.Asp120=
NM_001110221.3:c.358G=	NP_001103691.1:p.Asp120=
NM_006783.5:c.358G=	NP_006774.2:p.Asp120=