Canonical Allele Identifier: CA8370553

Gene: TMEM107

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8173448G>A , CM000679.2:g.8173448G>A	GRCh38
NC_000017.10:g.8076766G>A , CM000679.1:g.8076766G>A	GRCh37
NC_000017.9:g.8017491G>A	NCBI36
NG_054916.1:g.7964C>T
NG_056674.1:g.5141C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_183065.4:c.*755C>T MANE Select	NP_898888.1:n.*755C>T
ENST00000437139.7:c.*755C>T MANE Select	ENSP00000402732.2:n.*755C>T
NM_001351278.1:c.*755C>T	NP_001338207.1:n.*755C>T
NM_001351278.2:c.*755C>T	NP_001338207.1:n.*755C>T
NM_001351279.1:c.*755C>T	NP_001338208.1:n.*755C>T
NM_001351279.2:c.*755C>T	NP_001338208.1:n.*755C>T
NM_001351280.1:c.*755C>T	NP_001338209.1:n.*755C>T
NM_001351280.2:c.*755C>T	NP_001338209.1:n.*755C>T
NM_032354.3:c.*755C>T	NP_115730.2:n.*755C>T
NM_032354.4:c.*755C>T	NP_115730.2:n.*755C>T
NM_032354.5:c.*755C>T	NP_115730.2:n.*755C>T
NM_183065.2:c.*755C>T	NP_898888.1:n.*755C>T
NM_183065.3:c.*755C>T	NP_898888.1:n.*755C>T
NR_147092.1:n.1037C>T
NR_147092.2:n.1006C>T
ENST00000449985.6:c.*804C>T	ENSP00000404753.2:n.*804C>T