Canonical Allele Identifier: CA2526267236

Gene: TMEM132C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701547C>T , CM000674.2:g.128701547C>T	GRCh38
NC_000012.11:g.129186092C>T , CM000674.1:g.129186092C>T	GRCh37
NC_000012.10:g.127752045C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000435159.3:c.2122-3543C>T MANE Select	ENSP00000410852.2:n.2122-3543C>T
ENST00000435159.2:c.2122-3543C>T	ENSP00000410852.2:n.2122-3543C>T
NM_001136103.2:c.2122-3543C>T	NP_001129575.2:n.2122-3543C>T
XM_011538998.1:c.2062-3543C>T	XP_011537300.1:n.2062-3543C>T
XM_011538998.2:c.2062-3543C>T	XP_011537300.1:n.2062-3543C>T
XR_001748922.1:n.2355-3105C>T
NM_001136103.3:c.2122-3543C>T MANE Select	NP_001129575.2:n.2122-3543C>T
NM_001387058.1:c.2062-3543C>T	NP_001373987.1:n.2062-3543C>T