Canonical Allele Identifier: CA608311037

Gene: TMEM132B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.125658800G>T , CM000674.2:g.125658800G>T	GRCh38
NC_000012.11:g.126143346G>T , CM000674.1:g.126143346G>T	GRCh37
NC_000012.10:g.124709299G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682704.1:c.*4090G>T MANE Select	ENSP00000507790.1:n.*4090G>T
ENST00000299308.7:c.*4090G>T	ENSP00000299308.3:n.*4090G>T
ENST00000613307.1:c.*4090G>T	ENSP00000482788.1:n.*4090G>T
NM_001286219.1:c.*4090G>T	NP_001273148.1:n.*4090G>T
NM_052907.3:c.*4090G>T	NP_443139.2:n.*4090G>T
XM_011537852.1:c.*4090G>T	XP_011536154.1:n.*4090G>T
XM_011537853.1:c.*4090G>T	XP_011536155.1:n.*4090G>T
XM_011537854.1:c.*4090G>T	XP_011536156.1:n.*4090G>T
NM_001366854.1:c.*4090G>T MANE Select	NP_001353783.1:n.*4090G>T
XM_011537854.2:c.*4090G>T	XP_011536156.1:n.*4090G>T
XM_017018767.1:c.*4090G>T	XP_016874256.1:n.*4090G>T
NM_001286219.2:c.*4090G>T	NP_001273148.1:n.*4090G>T