Canonical Allele Identifier: CA2797949123

Gene: TMEM132C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701820_128701821insAGT , CM000674.2:g.128701820_128701821insAGT	GRCh38
NC_000012.11:g.129186365_129186366insAGT , CM000674.1:g.129186365_129186366insAGT	GRCh37
NC_000012.10:g.127752318_127752319insAGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3270_2122-3269insAGT MANE Select	ENSP00000410852.2:n.2122-3270_2122-3269insAGT
ENST00000435159.2:c.2122-3270_2122-3269insAGT	ENSP00000410852.2:n.2122-3270_2122-3269insAGT
NM_001136103.2:c.2122-3270_2122-3269insAGT	NP_001129575.2:n.2122-3270_2122-3269insAGT
XM_011538998.1:c.2062-3270_2062-3269insAGT	XP_011537300.1:n.2062-3270_2062-3269insAGT
XM_011538998.2:c.2062-3270_2062-3269insAGT	XP_011537300.1:n.2062-3270_2062-3269insAGT
XR_001748922.1:n.2355-2832_2355-2831insAGT
NM_001136103.3:c.2122-3270_2122-3269insAGT MANE Select	NP_001129575.2:n.2122-3270_2122-3269insAGT
NM_001387058.1:c.2062-3270_2062-3269insAGT	NP_001373987.1:n.2062-3270_2062-3269insAGT