Canonical Allele Identifier: CA15310828
Gene: TMEM165 HGNC NCBI

Linked Data

dbSNP Id: rs11943456
gnomAD v2: 4-56276334-T-C
gnomAD v3: 4-55410167-T-C
gnomAD v4: 4-55410167-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55410167T>C , CM000666.2:g.55410167T>C GRCh38
NC_000004.11:g.56276334T>C , CM000666.1:g.56276334T>C GRCh37
NC_000004.10:g.55971091T>C NCBI36
NG_032881.1:g.19255T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000381334.10:c.208-1447T>C MANE Select ENSP00000370736.5:n.208-1447T>C
ENST00000381334.9:c.208-1447T>C ENSP00000370736.5:n.208-1447T>C
ENST00000502797.1:n.97-1447T>C
ENST00000506198.5:c.207+13771T>C ENSP00000425449.1:n.207+13771T>C
ENST00000508404.5:c.*80-1447T>C ENSP00000422639.1:n.*80-1447T>C
ENST00000511710.1:n.332-1447T>C
NM_018475.4:c.208-1447T>C NP_060945.2:n.208-1447T>C
NR_073070.1:n.588-1447T>C
XM_011534394.1:c.208-1447T>C XP_011532696.1:n.208-1447T>C
XM_011534394.3:c.208-1447T>C XP_011532696.1:n.208-1447T>C
XM_017008412.1:c.19-1447T>C XP_016863901.1:n.19-1447T>C
XR_001741287.2:n.745-1447T>C
NM_018475.5:c.208-1447T>C MANE Select NP_060945.2:n.208-1447T>C
NR_073070.2:n.544-1447T>C