Canonical Allele Identifier: CA14121397

Gene: SEMA7A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74424268A>G , CM000677.2:g.74424268A>G	GRCh38
NC_000015.9:g.74716609A>G , CM000677.1:g.74716609A>G	GRCh37
NC_000015.8:g.72503662A>G	NCBI36
NG_011733.1:g.14691T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.179-5316T>C MANE Select	ENSP00000261918.4:n.179-5316T>C
ENST00000542748.6:c.-317-5316T>C	ENSP00000441493.1:n.-317-5316T>C
ENST00000261918.8:c.179-5316T>C	ENSP00000261918.4:n.179-5316T>C
ENST00000542748.5:c.-317-5316T>C	ENSP00000441493.1:n.-317-5316T>C
ENST00000543145.6:c.179-5316T>C	ENSP00000438966.2:n.179-5316T>C
ENST00000567345.1:c.-317-5316T>C	ENSP00000454365.1:n.-317-5316T>C
NM_001146029.1:c.179-5316T>C	NP_001139501.1:n.179-5316T>C
NM_001146030.1:c.-317-5316T>C	NP_001139502.1:n.-317-5316T>C
NM_003612.3:c.179-5316T>C	NP_003603.1:n.179-5316T>C
NM_001146029.2:c.179-5316T>C	NP_001139501.1:n.179-5316T>C
NM_001146030.2:c.-317-5316T>C	NP_001139502.1:n.-317-5316T>C
NM_003612.4:c.179-5316T>C	NP_003603.1:n.179-5316T>C
NM_003612.5:c.179-5316T>C MANE Select	NP_003603.1:n.179-5316T>C
NM_001146029.3:c.179-5316T>C	NP_001139501.1:n.179-5316T>C
NM_001146030.3:c.-317-5316T>C	NP_001139502.1:n.-317-5316T>C