Canonical Allele Identifier: CA2629481907

Gene: SEMA7A

Linked Data

• gnomAD v4: 15-74418159-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74418160_74418161insCC , CM000677.2:g.74418160_74418161insCC	GRCh38
NC_000015.9:g.74710501_74710502insCC , CM000677.1:g.74710501_74710502insCC	GRCh37
NC_000015.8:g.72497554_72497555insCC	NCBI36
NG_011733.1:g.20799_20800insGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261918.9:c.372+108_372+109insGG MANE Select	ENSP00000261918.4:n.372+108_372+109insGG
ENST00000542748.6:c.-124+108_-124+109insGG	ENSP00000441493.1:n.-124+108_-124+109insG...
ENST00000261918.8:c.372+108_372+109insGG	ENSP00000261918.4:n.372+108_372+109insGG
ENST00000542748.5:c.-124+108_-124+109insGG	ENSP00000441493.1:n.-124+108_-124+109insG...
ENST00000543145.6:c.331-191_331-190insGG	ENSP00000438966.2:n.331-191_331-190insGG
ENST00000567345.1:c.-124+108_-124+109insGG	ENSP00000454365.1:n.-124+108_-124+109insG...
NM_001146029.1:c.331-191_331-190insGG	NP_001139501.1:n.331-191_331-190insGG
NM_001146030.1:c.-124+108_-124+109insGG	NP_001139502.1:n.-124+108_-124+109insGG
NM_003612.3:c.372+108_372+109insGG	NP_003603.1:n.372+108_372+109insGG
NM_001146029.2:c.331-191_331-190insGG	NP_001139501.1:n.331-191_331-190insGG
NM_001146030.2:c.-124+108_-124+109insGG	NP_001139502.1:n.-124+108_-124+109insGG
NM_003612.4:c.372+108_372+109insGG	NP_003603.1:n.372+108_372+109insGG
NM_003612.5:c.372+108_372+109insGG MANE Select	NP_003603.1:n.372+108_372+109insGG
NM_001146029.3:c.331-191_331-190insGG	NP_001139501.1:n.331-191_331-190insGG
NM_001146030.3:c.-124+108_-124+109insGG	NP_001139502.1:n.-124+108_-124+109insGG