Canonical Allele Identifier: CA2071304409
Gene: TMEM132C HGNC NCBI

Linked Data

dbSNP Id: rs1593119456
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128610499A>C , CM000674.2:g.128610499A>C GRCh38
NC_000012.11:g.129095044A>C , CM000674.1:g.129095044A>C GRCh37
NC_000012.10:g.127660997A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435159.3:c.1122-5653A>C MANE Select ENSP00000410852.2:n.1122-5653A>C
ENST00000435159.2:c.1122-5653A>C ENSP00000410852.2:n.1122-5653A>C
NM_001136103.2:c.1122-5653A>C NP_001129575.2:n.1122-5653A>C
XM_011538998.1:c.1062-5653A>C XP_011537300.1:n.1062-5653A>C
XM_011538998.2:c.1062-5653A>C XP_011537300.1:n.1062-5653A>C
XR_001748922.1:n.1355-5653A>C
NM_001136103.3:c.1122-5653A>C MANE Select NP_001129575.2:n.1122-5653A>C
NM_001387058.1:c.1062-5653A>C NP_001373987.1:n.1062-5653A>C
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