Canonical Allele Identifier: CA2071351226

Gene: TMEM132C

Linked Data

• dbSNP Id: rs1954807670

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128702009_128702011del , CM000674.2:g.128702009_128702011del	GRCh38
NC_000012.11:g.129186554_129186556del , CM000674.1:g.129186554_129186556del	GRCh37
NC_000012.10:g.127752507_127752509del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3081_2122-3079del MANE Select	ENSP00000410852.2:n.2122-3081_2122-3079del
ENST00000435159.2:c.2122-3081_2122-3079del	ENSP00000410852.2:n.2122-3081_2122-3079del
NM_001136103.2:c.2122-3081_2122-3079del	NP_001129575.2:n.2122-3081_2122-3079del
XM_011538998.1:c.2062-3081_2062-3079del	XP_011537300.1:n.2062-3081_2062-3079del
XM_011538998.2:c.2062-3081_2062-3079del	XP_011537300.1:n.2062-3081_2062-3079del
XR_001748922.1:n.2355-2643_2355-2641del
NM_001136103.3:c.2122-3081_2122-3079del MANE Select	NP_001129575.2:n.2122-3081_2122-3079del
NM_001387058.1:c.2062-3081_2062-3079del	NP_001373987.1:n.2062-3081_2062-3079del