Canonical Allele Identifier: CA2797947548

Gene: TMEM132C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128610459G>T , CM000674.2:g.128610459G>T	GRCh38
NC_000012.11:g.129095004G>T , CM000674.1:g.129095004G>T	GRCh37
NC_000012.10:g.127660957G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.1122-5693G>T MANE Select	ENSP00000410852.2:n.1122-5693G>T
ENST00000435159.2:c.1122-5693G>T	ENSP00000410852.2:n.1122-5693G>T
NM_001136103.2:c.1122-5693G>T	NP_001129575.2:n.1122-5693G>T
XM_011538998.1:c.1062-5693G>T	XP_011537300.1:n.1062-5693G>T
XM_011538998.2:c.1062-5693G>T	XP_011537300.1:n.1062-5693G>T
XR_001748922.1:n.1355-5693G>T
NM_001136103.3:c.1122-5693G>T MANE Select	NP_001129575.2:n.1122-5693G>T
NM_001387058.1:c.1062-5693G>T	NP_001373987.1:n.1062-5693G>T