Canonical Allele Identifier: CA2549984055
Gene: TMEM132C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128701567_128701568insTTGG , CM000674.2:g.128701567_128701568insTTGG GRCh38
NC_000012.11:g.129186112_129186113insTTGG , CM000674.1:g.129186112_129186113insTTGG GRCh37
NC_000012.10:g.127752065_127752066insTTGG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435159.3:c.2122-3523_2122-3522insTTGG MANE Select ENSP00000410852.2:n.2122-3523_2122-3522in...
ENST00000435159.2:c.2122-3523_2122-3522insTTGG ENSP00000410852.2:n.2122-3523_2122-3522in...
NM_001136103.2:c.2122-3523_2122-3522insTTGG NP_001129575.2:n.2122-3523_2122-3522insTT...
XM_011538998.1:c.2062-3523_2062-3522insTTGG XP_011537300.1:n.2062-3523_2062-3522insTT...
XM_011538998.2:c.2062-3523_2062-3522insTTGG XP_011537300.1:n.2062-3523_2062-3522insTT...
XR_001748922.1:n.2355-3085_2355-3084insTTGG
NM_001136103.3:c.2122-3523_2122-3522insTTGG MANE Select NP_001129575.2:n.2122-3523_2122-3522insTT...
NM_001387058.1:c.2062-3523_2062-3522insTTGG NP_001373987.1:n.2062-3523_2062-3522insTT...