Canonical Allele Identifier: CA2603964051
Gene: TMEM132C HGNC NCBI

Linked Data

gnomAD v3: 12-128610517-C-G
gnomAD v4: 12-128610517-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128610517C>G , CM000674.2:g.128610517C>G GRCh38
NC_000012.11:g.129095062C>G , CM000674.1:g.129095062C>G GRCh37
NC_000012.10:g.127661015C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435159.3:c.1122-5635C>G MANE Select ENSP00000410852.2:n.1122-5635C>G
ENST00000435159.2:c.1122-5635C>G ENSP00000410852.2:n.1122-5635C>G
NM_001136103.2:c.1122-5635C>G NP_001129575.2:n.1122-5635C>G
XM_011538998.1:c.1062-5635C>G XP_011537300.1:n.1062-5635C>G
XM_011538998.2:c.1062-5635C>G XP_011537300.1:n.1062-5635C>G
XR_001748922.1:n.1355-5635C>G
NM_001136103.3:c.1122-5635C>G MANE Select NP_001129575.2:n.1122-5635C>G
NM_001387058.1:c.1062-5635C>G NP_001373987.1:n.1062-5635C>G
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