Canonical Allele Identifier: CA2071304249

Gene: TMEM132C

Linked Data

• dbSNP Id: rs529725120

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128610394G>T , CM000674.2:g.128610394G>T	GRCh38
NC_000012.11:g.129094939G>T , CM000674.1:g.129094939G>T	GRCh37
NC_000012.10:g.127660892G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.1122-5758G>T MANE Select	ENSP00000410852.2:n.1122-5758G>T
ENST00000435159.2:c.1122-5758G>T	ENSP00000410852.2:n.1122-5758G>T
NM_001136103.2:c.1122-5758G>T	NP_001129575.2:n.1122-5758G>T
XM_011538998.1:c.1062-5758G>T	XP_011537300.1:n.1062-5758G>T
XM_011538998.2:c.1062-5758G>T	XP_011537300.1:n.1062-5758G>T
XR_001748922.1:n.1355-5758G>T
NM_001136103.3:c.1122-5758G>T MANE Select	NP_001129575.2:n.1122-5758G>T
NM_001387058.1:c.1062-5758G>T	NP_001373987.1:n.1062-5758G>T