Canonical Allele Identifier: CA2071351180

Gene: TMEM132C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701915_128701918delinsTTTG , CM000674.2:g.128701915_128701918delinsTTTG	GRCh38
NC_000012.11:g.129186460_129186463delinsTTTG , CM000674.1:g.129186460_129186463delinsTTTG	GRCh37
NC_000012.10:g.127752413_127752416delinsTTTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3175_2122-3172delinsTTTG MANE Select	ENSP00000410852.2:n.2122-3175_2122-3172delinsTTTG
ENST00000435159.2:c.2122-3175_2122-3172delinsTTTG	ENSP00000410852.2:n.2122-3175_2122-3172delinsTTTG
NM_001136103.2:c.2122-3175_2122-3172delinsTTTG	NP_001129575.2:n.2122-3175_2122-3172delinsTTTG
XM_011538998.1:c.2062-3175_2062-3172delinsTTTG	XP_011537300.1:n.2062-3175_2062-3172delinsTTTG
XM_011538998.2:c.2062-3175_2062-3172delinsTTTG	XP_011537300.1:n.2062-3175_2062-3172delinsTTTG
XR_001748922.1:n.2355-2737_2355-2734delinsTTTG
NM_001136103.3:c.2122-3175_2122-3172delinsTTTG MANE Select	NP_001129575.2:n.2122-3175_2122-3172delinsTTTG
NM_001387058.1:c.2062-3175_2062-3172delinsTTTG	NP_001373987.1:n.2062-3175_2062-3172delinsTTTG