Canonical Allele Identifier: CA1022403389

Gene: IGSF5

Linked Data

• dbSNP Id: rs2080147575
• gnomAD v3: 21-39777604-CTCTA-C
• gnomAD v4: 21-39777604-CTCTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.39777610_39777613del , CM000683.2:g.39777610_39777613del	GRCh38
NC_000021.8:g.41149537_41149540del , CM000683.1:g.41149537_41149540del	GRCh37
NC_000021.7:g.40071407_40071410del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380588.5:c.719-1480_719-1477del MANE Select	ENSP00000369962.4:n.719-1480_719-1477del
ENST00000380588.4:c.719-1480_719-1477del	ENSP00000369962.4:n.719-1480_719-1477del
ENST00000479378.1:n.825-1480_825-1477del
NM_001080444.1:c.719-1480_719-1477del	NP_001073913.1:n.719-1480_719-1477del
XM_011529472.1:c.989-1480_989-1477del	XP_011527774.1:n.989-1480_989-1477del
XM_011529473.1:c.989-1480_989-1477del	XP_011527775.1:n.989-1480_989-1477del
XM_011529472.2:c.989-1480_989-1477del	XP_011527774.1:n.989-1480_989-1477del
NM_001080444.2:c.719-1480_719-1477del MANE Select	NP_001073913.1:n.719-1480_719-1477del