Canonical Allele Identifier: CA15078879

Gene: TMCO1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165767643C>T , CM000663.2:g.165767643C>T	GRCh38
NC_000001.10:g.165736880C>T , CM000663.1:g.165736880C>T	GRCh37
NC_000001.9:g.164003504C>T	NCBI36
NG_032004.1:g.6280G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367881.11:c.148+549G>A MANE Select	ENSP00000356856.6:n.148+549G>A
ENST00000465705.4:c.148+549G>A	ENSP00000463105.2:n.148+549G>A
ENST00000476143.7:c.148+549G>A	ENSP00000464127.2:n.148+549G>A
ENST00000367881.9:c.301+549G>A	ENSP00000356856.5:n.301+549G>A
ENST00000392129.10:c.148+549G>A	ENSP00000375975.5:n.148+549G>A
ENST00000464650.5:c.-105+549G>A	ENSP00000463951.1:n.-105+549G>A
ENST00000465705.3:c.301+549G>A	ENSP00000463105.1:n.301+549G>A
ENST00000476143.6:c.285+549G>A
ENST00000481278.5:c.112+549G>A	ENSP00000462300.1:n.112+549G>A
ENST00000580248.5:c.-105+549G>A	ENSP00000462588.1:n.-105+549G>A
ENST00000612311.4:c.301+549G>A	ENSP00000480514.1:n.301+549G>A
ENST00000628579.1:c.301+549G>A	ENSP00000485789.1:n.301+549G>A
NM_001256164.1:c.199+549G>A	NP_001243093.1:n.199+549G>A
NM_001256165.1:c.112+549G>A	NP_001243094.1:n.112+549G>A
NM_019026.4:c.301+549G>A	NP_061899.2:n.301+549G>A
NR_045818.1:n.242+549G>A
NM_001366129.1:c.148+549G>A	NP_001353058.1:n.148+549G>A
NM_019026.5:c.148+549G>A	NP_061899.3:n.148+549G>A
NM_019026.6:c.148+549G>A MANE Select	NP_061899.3:n.148+549G>A