Canonical Allele Identifier: CA2797949135

Gene: TMEM132C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128702024T>A , CM000674.2:g.128702024T>A	GRCh38
NC_000012.11:g.129186569T>A , CM000674.1:g.129186569T>A	GRCh37
NC_000012.10:g.127752522T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3066T>A MANE Select	ENSP00000410852.2:n.2122-3066T>A
ENST00000435159.2:c.2122-3066T>A	ENSP00000410852.2:n.2122-3066T>A
NM_001136103.2:c.2122-3066T>A	NP_001129575.2:n.2122-3066T>A
XM_011538998.1:c.2062-3066T>A	XP_011537300.1:n.2062-3066T>A
XM_011538998.2:c.2062-3066T>A	XP_011537300.1:n.2062-3066T>A
XR_001748922.1:n.2355-2628T>A
NM_001136103.3:c.2122-3066T>A MANE Select	NP_001129575.2:n.2122-3066T>A
NM_001387058.1:c.2062-3066T>A	NP_001373987.1:n.2062-3066T>A