Canonical Allele Identifier: CA953178792

Gene: TMEM132C

Linked Data

• dbSNP Id: rs1954806998
• gnomAD v3: 12-128701914-TTTTG-T
• gnomAD v4: 12-128701914-TTTTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701915_128701918del , CM000674.2:g.128701915_128701918del	GRCh38
NC_000012.11:g.129186460_129186463del , CM000674.1:g.129186460_129186463del	GRCh37
NC_000012.10:g.127752413_127752416del	NCBI36

Transcript Alleles

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