Canonical Allele Identifier: CA2071351250

Gene: TMEM132C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128702060C= , CM000674.2:g.128702060C=	GRCh38
NC_000012.11:g.129186605C= , CM000674.1:g.129186605C=	GRCh37
NC_000012.10:g.127752558C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3030C= MANE Select	ENSP00000410852.2:n.2122-3030C=
ENST00000435159.2:c.2122-3030C=	ENSP00000410852.2:n.2122-3030C=
NM_001136103.2:c.2122-3030C=	NP_001129575.2:n.2122-3030C=
XM_011538998.1:c.2062-3030C=	XP_011537300.1:n.2062-3030C=
XM_011538998.2:c.2062-3030C=	XP_011537300.1:n.2062-3030C=
XR_001748922.1:n.2355-2592C=
NM_001136103.3:c.2122-3030C= MANE Select	NP_001129575.2:n.2122-3030C=
NM_001387058.1:c.2062-3030C=	NP_001373987.1:n.2062-3030C=