Canonical Allele Identifier: CA1855106322

Gene: TMC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72789234T= , CM000671.2:g.72789234T=	GRCh38
NC_000009.11:g.75404150T= , CM000671.1:g.75404150T=	GRCh37
NC_000009.10:g.74593970T=	NCBI36
NG_008213.1:g.272434T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1141T= MANE Select	ENSP00000297784.6:p.Tyr381=
ENST00000644967.1:c.703T=	ENSP00000496159.1:p.Tyr235=
ENST00000645053.1:c.703T=	ENSP00000493838.1:p.Tyr235=
ENST00000645208.2:c.1141T=	ENSP00000494684.1:p.Tyr381=
ENST00000645773.1:c.1015T=	ENSP00000493698.1:p.Tyr339=
ENST00000645787.1:n.1181T=
ENST00000646619.1:c.703T=	ENSP00000493726.1:p.Tyr235=
ENST00000650689.1:n.1439T=
ENST00000651183.1:c.703T=	ENSP00000498723.1:p.Tyr235=
ENST00000297784.9:c.1141T=	ENSP00000297784.5:p.Tyr381=
ENST00000340019.4:c.1141T=	ENSP00000341433.3:p.Tyr381=
NM_138691.2:c.1141T=	NP_619636.2:p.Tyr381=
XM_011518213.1:c.1729T=	XP_011516515.1:p.Tyr577=
XM_017014256.1:c.1144T=	XP_016869745.1:p.Tyr382=
NM_138691.3:c.1141T= MANE Select	NP_619636.2:p.Tyr381=