Canonical Allele Identifier: CA1855120664

Gene: TMC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72820917C= , CM000671.2:g.72820917C=	GRCh38
NC_000009.11:g.75435833C= , CM000671.1:g.75435833C=	GRCh37
NC_000009.10:g.74625653C=	NCBI36
NG_008213.1:g.304117C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1839C= MANE Select	ENSP00000297784.6:p.Cys613=
ENST00000644967.1:c.*279C=	ENSP00000496159.1:n.*279C=
ENST00000645053.1:c.1258-5952C=	ENSP00000493838.1:n.1258-5952C=
ENST00000645208.2:c.1839C=	ENSP00000494684.1:p.Cys613=
ENST00000645773.1:c.1713C=	ENSP00000493698.1:p.Cys571=
ENST00000645787.1:n.1982C=
ENST00000646619.1:c.1401C=	ENSP00000493726.1:p.Cys467=
ENST00000651183.1:c.1401C=	ENSP00000498723.1:p.Cys467=
ENST00000297784.9:c.1839C=	ENSP00000297784.5:p.Cys613=
ENST00000340019.4:c.1839C=	ENSP00000341433.3:p.Cys613=
ENST00000469455.1:n.320C=
ENST00000486417.5:n.737C=
NM_138691.2:c.1839C=	NP_619636.2:p.Cys613=
XM_011518213.1:c.2427C=	XP_011516515.1:p.Cys809=
XM_017014256.1:c.1842C=	XP_016869745.1:p.Cys614=
NM_138691.3:c.1839C= MANE Select	NP_619636.2:p.Cys613=