Canonical Allele Identifier: CA31904610

Gene: TMCO1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165754533A>G , CM000663.2:g.165754533A>G	GRCh38
NC_000001.10:g.165723770A>G , CM000663.1:g.165723770A>G	GRCh37
NC_000001.9:g.163990394A>G	NCBI36
NG_032004.1:g.19390T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367881.11:c.209-259T>C MANE Select	ENSP00000356856.6:n.209-259T>C
ENST00000465705.4:c.*40-259T>C	ENSP00000463105.2:n.*40-259T>C
ENST00000476143.7:c.149-259T>C	ENSP00000464127.2:n.149-259T>C
ENST00000367881.9:c.362-259T>C	ENSP00000356856.5:n.362-259T>C
ENST00000392129.10:c.209-259T>C	ENSP00000375975.5:n.209-259T>C
ENST00000464650.5:c.-44-259T>C	ENSP00000463951.1:n.-44-259T>C
ENST00000465705.3:c.*40-259T>C	ENSP00000463105.1:n.*40-259T>C
ENST00000476143.6:c.286-259T>C
ENST00000481278.5:c.173-259T>C	ENSP00000462300.1:n.173-259T>C
ENST00000580248.5:c.-44-259T>C	ENSP00000462588.1:n.-44-259T>C
ENST00000612311.4:c.362-259T>C	ENSP00000480514.1:n.362-259T>C
NM_001256164.1:c.260-259T>C	NP_001243093.1:n.260-259T>C
NM_001256165.1:c.173-259T>C	NP_001243094.1:n.173-259T>C
NM_019026.4:c.362-259T>C	NP_061899.2:n.362-259T>C
NR_045818.1:n.303-259T>C
NM_001366129.1:c.209-259T>C	NP_001353058.1:n.209-259T>C
NM_019026.5:c.209-259T>C	NP_061899.3:n.209-259T>C
NM_019026.6:c.209-259T>C MANE Select	NP_061899.3:n.209-259T>C