Canonical Allele Identifier: CA15754163

Gene: TMEM132C

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128360026T>C , CM000674.2:g.128360026T>C	GRCh38
NC_000012.11:g.128844571T>C , CM000674.1:g.128844571T>C	GRCh37
NC_000012.10:g.127410524T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.86-54706T>C MANE Select	ENSP00000410852.2:n.86-54706T>C
ENST00000435159.2:c.86-54706T>C	ENSP00000410852.2:n.86-54706T>C
NM_001136103.2:c.86-54706T>C	NP_001129575.2:n.86-54706T>C
XM_011538998.1:c.26-54706T>C	XP_011537300.1:n.26-54706T>C
XM_011538998.2:c.26-54706T>C	XP_011537300.1:n.26-54706T>C
XR_001748922.1:n.319-54706T>C
NM_001136103.3:c.86-54706T>C MANE Select	NP_001129575.2:n.86-54706T>C
NM_001387058.1:c.26-54706T>C	NP_001373987.1:n.26-54706T>C