Canonical Allele Identifier: CA2071351158

Gene: TMEM132C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701896_128701901delinsCTTCTT , CM000674.2:g.128701896_128701901delinsCTTCTT	GRCh38
NC_000012.11:g.129186441_129186446delinsCTTCTT , CM000674.1:g.129186441_129186446delinsCTTCTT	GRCh37
NC_000012.10:g.127752394_127752399delinsCTTCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3194_2122-3189delinsCTTCTT MANE Select	ENSP00000410852.2:n.2122-3194_2122-3189delinsCTTCTT
ENST00000435159.2:c.2122-3194_2122-3189delinsCTTCTT	ENSP00000410852.2:n.2122-3194_2122-3189delinsCTTCTT
NM_001136103.2:c.2122-3194_2122-3189delinsCTTCTT	NP_001129575.2:n.2122-3194_2122-3189delinsCTTCTT
XM_011538998.1:c.2062-3194_2062-3189delinsCTTCTT	XP_011537300.1:n.2062-3194_2062-3189delinsCTTCTT
XM_011538998.2:c.2062-3194_2062-3189delinsCTTCTT	XP_011537300.1:n.2062-3194_2062-3189delinsCTTCTT
XR_001748922.1:n.2355-2756_2355-2751delinsCTTCTT
NM_001136103.3:c.2122-3194_2122-3189delinsCTTCTT MANE Select	NP_001129575.2:n.2122-3194_2122-3189delinsCTTCTT
NM_001387058.1:c.2062-3194_2062-3189delinsCTTCTT	NP_001373987.1:n.2062-3194_2062-3189delinsCTTCTT