Canonical Allele Identifier: CA2629481905

Gene: SEMA7A

Linked Data

• gnomAD v4: 15-74418158-A-ACGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74418158_74418159insCGAG , CM000677.2:g.74418158_74418159insCGAG	GRCh38
NC_000015.9:g.74710499_74710500insCGAG , CM000677.1:g.74710499_74710500insCGAG	GRCh37
NC_000015.8:g.72497552_72497553insCGAG	NCBI36
NG_011733.1:g.20800_20801insCTCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261918.9:c.372+109_372+110insCTCG MANE Select	ENSP00000261918.4:n.372+109_372+110insCTC...
ENST00000542748.6:c.-124+109_-124+110insCTCG	ENSP00000441493.1:n.-124+109_-124+110insC...
ENST00000261918.8:c.372+109_372+110insCTCG	ENSP00000261918.4:n.372+109_372+110insCTC...
ENST00000542748.5:c.-124+109_-124+110insCTCG	ENSP00000441493.1:n.-124+109_-124+110insC...
ENST00000543145.6:c.331-190_331-189insCTCG	ENSP00000438966.2:n.331-190_331-189insCTC...
ENST00000567345.1:c.-124+109_-124+110insCTCG	ENSP00000454365.1:n.-124+109_-124+110insC...
NM_001146029.1:c.331-190_331-189insCTCG	NP_001139501.1:n.331-190_331-189insCTCG
NM_001146030.1:c.-124+109_-124+110insCTCG	NP_001139502.1:n.-124+109_-124+110insCTCG...
NM_003612.3:c.372+109_372+110insCTCG	NP_003603.1:n.372+109_372+110insCTCG
NM_001146029.2:c.331-190_331-189insCTCG	NP_001139501.1:n.331-190_331-189insCTCG
NM_001146030.2:c.-124+109_-124+110insCTCG	NP_001139502.1:n.-124+109_-124+110insCTCG...
NM_003612.4:c.372+109_372+110insCTCG	NP_003603.1:n.372+109_372+110insCTCG
NM_003612.5:c.372+109_372+110insCTCG MANE Select	NP_003603.1:n.372+109_372+110insCTCG
NM_001146029.3:c.331-190_331-189insCTCG	NP_001139501.1:n.331-190_331-189insCTCG
NM_001146030.3:c.-124+109_-124+110insCTCG	NP_001139502.1:n.-124+109_-124+110insCTCG...