Canonical Allele Identifier: CA2071351177

Gene: TMEM132C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701914_128701918delinsTTTTG , CM000674.2:g.128701914_128701918delinsTTTTG	GRCh38
NC_000012.11:g.129186459_129186463delinsTTTTG , CM000674.1:g.129186459_129186463delinsTTTTG	GRCh37
NC_000012.10:g.127752412_127752416delinsTTTTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3176_2122-3172delinsTTTTG MANE Select	ENSP00000410852.2:n.2122-3176_2122-3172delinsTTTTG
ENST00000435159.2:c.2122-3176_2122-3172delinsTTTTG	ENSP00000410852.2:n.2122-3176_2122-3172delinsTTTTG
NM_001136103.2:c.2122-3176_2122-3172delinsTTTTG	NP_001129575.2:n.2122-3176_2122-3172delinsTTTTG
XM_011538998.1:c.2062-3176_2062-3172delinsTTTTG	XP_011537300.1:n.2062-3176_2062-3172delinsTTTTG
XM_011538998.2:c.2062-3176_2062-3172delinsTTTTG	XP_011537300.1:n.2062-3176_2062-3172delinsTTTTG
XR_001748922.1:n.2355-2738_2355-2734delinsTTTTG
NM_001136103.3:c.2122-3176_2122-3172delinsTTTTG MANE Select	NP_001129575.2:n.2122-3176_2122-3172delinsTTTTG
NM_001387058.1:c.2062-3176_2062-3172delinsTTTTG	NP_001373987.1:n.2062-3176_2062-3172delinsTTTTG