Canonical Allele Identifier: CA2657109814

Gene: TSPO

Linked Data

• gnomAD v4: 22-43163204-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43163204G>T , CM000684.2:g.43163204G>T	GRCh38
NC_000022.10:g.43559210G>T , CM000684.1:g.43559210G>T	GRCh37
NC_000022.9:g.41889154G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.*213G>T MANE Select	ENSP00000338004.3:n.*213G>T
ENST00000329563.8:c.*213G>T	ENSP00000328973.4:n.*213G>T
ENST00000337554.7:c.*213G>T	ENSP00000338004.3:n.*213G>T
ENST00000396265.4:c.*213G>T	ENSP00000379563.4:n.*213G>T
ENST00000583777.5:c.*213G>T	ENSP00000463495.1:n.*213G>T
NM_000714.5:c.*213G>T	NP_000705.2:n.*213G>T
NM_001256530.1:c.*213G>T	NP_001243459.1:n.*213G>T
NM_001256531.1:c.*213G>T	NP_001243460.1:n.*213G>T
NR_046308.1:n.632G>T
NM_000714.6:c.*213G>T MANE Select	NP_000705.2:n.*213G>T
NR_046308.2:n.587G>T