Canonical Allele Identifier: CA1125391263

Gene: TMC1

Linked Data

• gnomAD v3: 9-72805554-TTTA-T
• gnomAD v4: 9-72805554-TTTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72805557_72805559del , CM000671.2:g.72805557_72805559del	GRCh38
NC_000009.11:g.75420473_75420475del , CM000671.1:g.75420473_75420475del	GRCh37
NC_000009.10:g.74610293_74610295del	NCBI36
NG_008213.1:g.288757_288759del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1695+47_1695+49del MANE Select	ENSP00000297784.6:n.1695+47_1695+49del
ENST00000644967.1:c.1257+47_1257+49del	ENSP00000496159.1:n.1257+47_1257+49del
ENST00000645053.1:c.1257+47_1257+49del	ENSP00000493838.1:n.1257+47_1257+49del
ENST00000645208.2:c.1695+47_1695+49del	ENSP00000494684.1:n.1695+47_1695+49del
ENST00000645773.1:c.1569+47_1569+49del	ENSP00000493698.1:n.1569+47_1569+49del
ENST00000645787.1:n.1838+47_1838+49del
ENST00000646619.1:c.1257+47_1257+49del	ENSP00000493726.1:n.1257+47_1257+49del
ENST00000651183.1:c.1257+47_1257+49del	ENSP00000498723.1:n.1257+47_1257+49del
ENST00000297784.9:c.1695+47_1695+49del	ENSP00000297784.5:n.1695+47_1695+49del
ENST00000340019.4:c.1695+47_1695+49del	ENSP00000341433.3:n.1695+47_1695+49del
ENST00000486417.5:n.319+47_319+49del
NM_138691.2:c.1695+47_1695+49del	NP_619636.2:n.1695+47_1695+49del
XM_011518213.1:c.2283+47_2283+49del	XP_011516515.1:n.2283+47_2283+49del
XM_017014256.1:c.1698+47_1698+49del	XP_016869745.1:n.1698+47_1698+49del
NM_138691.3:c.1695+47_1695+49del MANE Select	NP_619636.2:n.1695+47_1695+49del