Canonical Allele Identifier: CA2071351248
Gene: TMEM132C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128702056T= , CM000674.2:g.128702056T= GRCh38
NC_000012.11:g.129186601T= , CM000674.1:g.129186601T= GRCh37
NC_000012.10:g.127752554T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435159.3:c.2122-3034T= MANE Select ENSP00000410852.2:n.2122-3034T=
ENST00000435159.2:c.2122-3034T= ENSP00000410852.2:n.2122-3034T=
NM_001136103.2:c.2122-3034T= NP_001129575.2:n.2122-3034T=
XM_011538998.1:c.2062-3034T= XP_011537300.1:n.2062-3034T=
XM_011538998.2:c.2062-3034T= XP_011537300.1:n.2062-3034T=
XR_001748922.1:n.2355-2596T=
NM_001136103.3:c.2122-3034T= MANE Select NP_001129575.2:n.2122-3034T=
NM_001387058.1:c.2062-3034T= NP_001373987.1:n.2062-3034T=
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