Canonical Allele Identifier: CA953178562

Gene: TMEM132C

Linked Data

• dbSNP Id: rs1954803289
• gnomAD v3: 12-128701480-GCTA-G
• gnomAD v4: 12-128701480-GCTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701482_128701484del , CM000674.2:g.128701482_128701484del	GRCh38
NC_000012.11:g.129186027_129186029del , CM000674.1:g.129186027_129186029del	GRCh37
NC_000012.10:g.127751980_127751982del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3608_2122-3606del MANE Select	ENSP00000410852.2:n.2122-3608_2122-3606del
ENST00000435159.2:c.2122-3608_2122-3606del	ENSP00000410852.2:n.2122-3608_2122-3606del
NM_001136103.2:c.2122-3608_2122-3606del	NP_001129575.2:n.2122-3608_2122-3606del
XM_011538998.1:c.2062-3608_2062-3606del	XP_011537300.1:n.2062-3608_2062-3606del
XM_011538998.2:c.2062-3608_2062-3606del	XP_011537300.1:n.2062-3608_2062-3606del
XR_001748922.1:n.2355-3170_2355-3168del
NM_001136103.3:c.2122-3608_2122-3606del MANE Select	NP_001129575.2:n.2122-3608_2122-3606del
NM_001387058.1:c.2062-3608_2062-3606del	NP_001373987.1:n.2062-3608_2062-3606del