Canonical Allele Identifier: CA2519211822
Gene: TMEM165 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55423961C>G , CM000666.2:g.55423961C>G GRCh38
NC_000004.11:g.56290128C>G , CM000666.1:g.56290128C>G GRCh37
NC_000004.10:g.55984885C>G NCBI36
NG_032881.1:g.33049C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381334.10:c.793-577C>G MANE Select ENSP00000370736.5:n.793-577C>G
ENST00000381334.9:c.793-577C>G ENSP00000370736.5:n.793-577C>G
ENST00000506103.2:c.247-577C>G
ENST00000506198.5:c.208-577C>G ENSP00000425449.1:n.208-577C>G
ENST00000508404.5:c.*665-577C>G ENSP00000422639.1:n.*665-577C>G
ENST00000508561.5:n.489-577C>G
ENST00000509575.1:n.296-577C>G
ENST00000514904.5:n.1247-577C>G
ENST00000515591.1:n.848C>G
ENST00000608091.1:c.303-577C>G
NM_018475.4:c.793-577C>G NP_060945.2:n.793-577C>G
NR_073070.1:n.1173-577C>G
XM_011534394.1:c.793-577C>G XP_011532696.1:n.793-577C>G
XM_011534394.3:c.793-577C>G XP_011532696.1:n.793-577C>G
XM_017008412.1:c.604-577C>G XP_016863901.1:n.604-577C>G
XR_001741287.2:n.1509-577C>G
NM_018475.5:c.793-577C>G MANE Select NP_060945.2:n.793-577C>G
NR_073070.2:n.1129-577C>G