Canonical Allele Identifier: CA2071351028
Gene: TMEM132C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128701599A= , CM000674.2:g.128701599A= GRCh38
NC_000012.11:g.129186144A= , CM000674.1:g.129186144A= GRCh37
NC_000012.10:g.127752097A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435159.3:c.2122-3491A= MANE Select ENSP00000410852.2:n.2122-3491A=
ENST00000435159.2:c.2122-3491A= ENSP00000410852.2:n.2122-3491A=
NM_001136103.2:c.2122-3491A= NP_001129575.2:n.2122-3491A=
XM_011538998.1:c.2062-3491A= XP_011537300.1:n.2062-3491A=
XM_011538998.2:c.2062-3491A= XP_011537300.1:n.2062-3491A=
XR_001748922.1:n.2355-3053A=
NM_001136103.3:c.2122-3491A= MANE Select NP_001129575.2:n.2122-3491A=
NM_001387058.1:c.2062-3491A= NP_001373987.1:n.2062-3491A=