Canonical Allele Identifier: CA465189402

Gene: TMC1

Linked Data

• gnomAD v4: 9-72700590-T-C
• MyVariant Identifiers: chr9:g.75315506T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72700590T>C , CM000671.2:g.72700590T>C	GRCh38
NC_000009.11:g.75315506T>C , CM000671.1:g.75315506T>C	GRCh37
NC_000009.10:g.74505326T>C	NCBI36
NG_008213.1:g.183790T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.309T>C MANE Select	ENSP00000297784.6:p.Ile103=
ENST00000644967.1:c.-77+5876T>C	ENSP00000496159.1:n.-77+5876T>C
ENST00000645053.1:c.-77+5876T>C	ENSP00000493838.1:n.-77+5876T>C
ENST00000645208.2:c.309T>C	ENSP00000494684.1:p.Ile103=
ENST00000645773.1:c.236+5876T>C	ENSP00000493698.1:n.236+5876T>C
ENST00000645787.1:n.349T>C
ENST00000646244.1:n.759T>C
ENST00000646619.1:c.-77+5876T>C	ENSP00000493726.1:n.-77+5876T>C
ENST00000650689.1:n.660+5876T>C
ENST00000651183.1:c.-77+5876T>C	ENSP00000498723.1:n.-77+5876T>C
ENST00000297784.9:c.309T>C	ENSP00000297784.5:p.Ile103=
ENST00000340019.4:c.309T>C	ENSP00000341433.3:p.Ile103=
NM_138691.2:c.309T>C	NP_619636.2:p.Ile103=
XM_011518213.1:c.897T>C	XP_011516515.1:p.Ile299=
XM_017014256.1:c.312T>C	XP_016869745.1:p.Ile104=
NM_138691.3:c.309T>C MANE Select	NP_619636.2:p.Ile103=