Canonical Allele Identifier: CA2519196509

Gene: TMEM132C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701902_128701903insC , CM000674.2:g.128701902_128701903insC	GRCh38
NC_000012.11:g.129186447_129186448insC , CM000674.1:g.129186447_129186448insC	GRCh37
NC_000012.10:g.127752400_127752401insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3188_2122-3187insC MANE Select	ENSP00000410852.2:n.2122-3188_2122-3187insC
ENST00000435159.2:c.2122-3188_2122-3187insC	ENSP00000410852.2:n.2122-3188_2122-3187insC
NM_001136103.2:c.2122-3188_2122-3187insC	NP_001129575.2:n.2122-3188_2122-3187insC
XM_011538998.1:c.2062-3188_2062-3187insC	XP_011537300.1:n.2062-3188_2062-3187insC
XM_011538998.2:c.2062-3188_2062-3187insC	XP_011537300.1:n.2062-3188_2062-3187insC
XR_001748922.1:n.2355-2750_2355-2749insC
NM_001136103.3:c.2122-3188_2122-3187insC MANE Select	NP_001129575.2:n.2122-3188_2122-3187insC
NM_001387058.1:c.2062-3188_2062-3187insC	NP_001373987.1:n.2062-3188_2062-3187insC