Canonical Allele Identifier: CA953178811

Gene: TMEM132C

Linked Data

• gnomAD v3: 12-128701917-T-TTTA
• gnomAD v4: 12-128701917-T-TTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701917_128701918insTTA , CM000674.2:g.128701917_128701918insTTA	GRCh38
NC_000012.11:g.129186462_129186463insTTA , CM000674.1:g.129186462_129186463insTTA	GRCh37
NC_000012.10:g.127752415_127752416insTTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3173_2122-3172insTTA MANE Select	ENSP00000410852.2:n.2122-3173_2122-3172insTTA
ENST00000435159.2:c.2122-3173_2122-3172insTTA	ENSP00000410852.2:n.2122-3173_2122-3172insTTA
NM_001136103.2:c.2122-3173_2122-3172insTTA	NP_001129575.2:n.2122-3173_2122-3172insTTA
XM_011538998.1:c.2062-3173_2062-3172insTTA	XP_011537300.1:n.2062-3173_2062-3172insTTA
XM_011538998.2:c.2062-3173_2062-3172insTTA	XP_011537300.1:n.2062-3173_2062-3172insTTA
XR_001748922.1:n.2355-2735_2355-2734insTTA
NM_001136103.3:c.2122-3173_2122-3172insTTA MANE Select	NP_001129575.2:n.2122-3173_2122-3172insTTA
NM_001387058.1:c.2062-3173_2062-3172insTTA	NP_001373987.1:n.2062-3173_2062-3172insTTA