Canonical Allele Identifier: CA608136457

Gene: TMEM132C

Linked Data

• dbSNP Id: rs1593154223
• gnomAD v2: 12-129186434-G-GCTT
• gnomAD v3: 12-128701889-G-GCTT
• gnomAD v4: 12-128701889-G-GCTT
• MyVariant Identifiers: chr12:g.129186434_129186435insCTT (hg19) ; chr12:g.128701889_128701890insCTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701899_128701901dup , CM000674.2:g.128701899_128701901dup	GRCh38
NC_000012.11:g.129186444_129186446dup , CM000674.1:g.129186444_129186446dup	GRCh37
NC_000012.10:g.127752397_127752399dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3191_2122-3189dup MANE Select	ENSP00000410852.2:n.2122-3191_2122-3189dup
ENST00000435159.2:c.2122-3191_2122-3189dup	ENSP00000410852.2:n.2122-3191_2122-3189dup
NM_001136103.2:c.2122-3191_2122-3189dup	NP_001129575.2:n.2122-3191_2122-3189dup
XM_011538998.1:c.2062-3191_2062-3189dup	XP_011537300.1:n.2062-3191_2062-3189dup
XM_011538998.2:c.2062-3191_2062-3189dup	XP_011537300.1:n.2062-3191_2062-3189dup
XR_001748922.1:n.2355-2753_2355-2751dup
NM_001136103.3:c.2122-3191_2122-3189dup MANE Select	NP_001129575.2:n.2122-3191_2122-3189dup
NM_001387058.1:c.2062-3191_2062-3189dup	NP_001373987.1:n.2062-3191_2062-3189dup