Canonical Allele Identifier: CA2071351190
Gene: TMEM132C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128701925A= , CM000674.2:g.128701925A= GRCh38
NC_000012.11:g.129186470A= , CM000674.1:g.129186470A= GRCh37
NC_000012.10:g.127752423A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435159.3:c.2122-3165A= MANE Select ENSP00000410852.2:n.2122-3165A=
ENST00000435159.2:c.2122-3165A= ENSP00000410852.2:n.2122-3165A=
NM_001136103.2:c.2122-3165A= NP_001129575.2:n.2122-3165A=
XM_011538998.1:c.2062-3165A= XP_011537300.1:n.2062-3165A=
XM_011538998.2:c.2062-3165A= XP_011537300.1:n.2062-3165A=
XR_001748922.1:n.2355-2727A=
NM_001136103.3:c.2122-3165A= MANE Select NP_001129575.2:n.2122-3165A=
NM_001387058.1:c.2062-3165A= NP_001373987.1:n.2062-3165A=
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