Canonical Allele Identifier: CA2071304476
Gene: TMEM132C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128610562A= , CM000674.2:g.128610562A= GRCh38
NC_000012.11:g.129095107A= , CM000674.1:g.129095107A= GRCh37
NC_000012.10:g.127661060A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435159.3:c.1122-5590A= MANE Select ENSP00000410852.2:n.1122-5590A=
ENST00000435159.2:c.1122-5590A= ENSP00000410852.2:n.1122-5590A=
NM_001136103.2:c.1122-5590A= NP_001129575.2:n.1122-5590A=
XM_011538998.1:c.1062-5590A= XP_011537300.1:n.1062-5590A=
XM_011538998.2:c.1062-5590A= XP_011537300.1:n.1062-5590A=
XR_001748922.1:n.1355-5590A=
NM_001136103.3:c.1122-5590A= MANE Select NP_001129575.2:n.1122-5590A=
NM_001387058.1:c.1062-5590A= NP_001373987.1:n.1062-5590A=