Canonical Allele Identifier: CA914696964

Gene: TSPO

Linked Data

• gnomAD v2: 22-43558820-TCTC-T
• gnomAD v4: 22-43162814-TCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162817_43162819del , CM000684.2:g.43162817_43162819del	GRCh38
NC_000022.10:g.43558823_43558825del , CM000684.1:g.43558823_43558825del	GRCh37
NC_000022.9:g.41888767_41888769del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.336_338del MANE Select	ENSP00000338004.3:p.Leu113del
ENST00000329563.8:c.336_338del	ENSP00000328973.4:p.Leu113del
ENST00000337554.7:c.336_338del	ENSP00000338004.3:p.Leu113del
ENST00000396265.4:c.336_338del	ENSP00000379563.4:p.Leu113del
ENST00000583777.5:c.24_26del	ENSP00000463495.1:p.Leu9del
NM_000714.5:c.336_338del	NP_000705.2:p.Leu113del
NM_001256530.1:c.336_338del	NP_001243459.1:p.Leu113del
NM_001256531.1:c.336_338del	NP_001243460.1:p.Leu113del
NR_046308.1:n.245_247del
NM_000714.6:c.336_338del MANE Select	NP_000705.2:p.Leu113del
NR_046308.2:n.200_202del