Canonical Allele Identifier: CA2694983328

Gene: NSDHL

Linked Data

• gnomAD v4: X-152867488-TCAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.152867489_152867491del , CM000685.2:g.152867489_152867491del	GRCh38
NC_000023.10:g.152036033_152036035del , CM000685.1:g.152036033_152036035del	GRCh37
NC_000023.9:g.151786689_151786691del	NCBI36
NG_009163.1:g.41523_41525del
NG_009163.2:g.41523_41525del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370274.8:c.687-82_687-80del MANE Select	ENSP00000359297.3:n.687-82_687-80del
ENST00000370274.7:c.687-82_687-80del	ENSP00000359297.3:n.687-82_687-80del
ENST00000432467.1:c.687-82_687-80del	ENSP00000396266.1:n.687-82_687-80del
ENST00000440023.5:c.687-82_687-80del	ENSP00000391854.1:n.687-82_687-80del
NM_001129765.1:c.687-82_687-80del	NP_001123237.1:n.687-82_687-80del
NM_015922.2:c.687-82_687-80del	NP_057006.1:n.687-82_687-80del
XM_011531178.1:c.687-82_687-80del	XP_011529480.1:n.687-82_687-80del
XM_011531178.2:c.687-82_687-80del	XP_011529480.1:n.687-82_687-80del
XM_017029564.1:c.735-82_735-80del	XP_016885053.1:n.735-82_735-80del
NM_015922.3:c.687-82_687-80del MANE Select	NP_057006.1:n.687-82_687-80del
NM_001129765.2:c.687-82_687-80del	NP_001123237.1:n.687-82_687-80del