Canonical Allele Identifier: CA842758192

Gene: SEMA3C

Linked Data

• dbSNP Id: rs1181251771
• gnomAD v3: 7-80902850-AGCCATTAGCCCATG-A
• gnomAD v4: 7-80902850-AGCCATTAGCCCATG-A
• MyVariant Identifiers: chr7:g.80532167_80532180del (hg19) ; chr7:g.80902851_80902864del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.80902853_80902866del , CM000669.2:g.80902853_80902866del	GRCh38
NC_000007.13:g.80532169_80532182del , CM000669.1:g.80532169_80532182del	GRCh37
NC_000007.12:g.80370105_80370118del	NCBI36
NG_054744.1:g.24516_24529del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265361.8:c.103+13815_103+13828del MANE Select	ENSP00000265361.3:n.103+13815_103+13828del
ENST00000265361.7:c.103+13815_103+13828del	ENSP00000265361.3:n.103+13815_103+13828del
ENST00000411788.5:c.191+2965_191+2978del	ENSP00000395398.1:n.191+2965_191+2978del
ENST00000419255.6:c.103+13815_103+13828del	ENSP00000411193.2:n.103+13815_103+13828del
ENST00000427167.5:c.191+2965_191+2978del	ENSP00000399891.1:n.191+2965_191+2978del
ENST00000458729.5:c.103+13815_103+13828del	ENSP00000393825.1:n.103+13815_103+13828del
ENST00000487621.5:n.496+13815_496+13828del
NM_006379.3:c.103+13815_103+13828del	NP_006370.1:n.103+13815_103+13828del
XM_005250113.1:c.-72+2965_-72+2978del	XP_005250170.1:n.-72+2965_-72+2978del
NM_001350120.1:c.157+13815_157+13828del	NP_001337049.1:n.157+13815_157+13828del
NM_001350121.1:c.-72+2965_-72+2978del	NP_001337050.1:n.-72+2965_-72+2978del
NM_006379.4:c.103+13815_103+13828del	NP_006370.1:n.103+13815_103+13828del
NM_006379.5:c.103+13815_103+13828del MANE Select	NP_006370.1:n.103+13815_103+13828del
NM_001350120.2:c.157+13815_157+13828del	NP_001337049.1:n.157+13815_157+13828del
NM_001350121.2:c.-72+2965_-72+2978del	NP_001337050.1:n.-72+2965_-72+2978del