Canonical Allele Identifier: CA16505388

Gene: SEMA6D

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.47389170G>A , CM000677.2:g.47389170G>A	GRCh38
NC_000015.9:g.47681367G>A , CM000677.1:g.47681367G>A	GRCh37
NC_000015.8:g.45468659G>A	NCBI36
NG_029119.1:g.209965G>A
NG_029119.2:g.209965G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001198999.1:c.-238-23223G>A	NP_001185928.1:n.-238-23223G>A
NM_001198999.2:c.-238-23223G>A	NP_001185928.1:n.-238-23223G>A
ENST00000558014.5:c.-238-23223G>A	ENSP00000452815.1:n.-238-23223G>A
ENST00000559184.5:c.-238-23223G>A	ENSP00000453097.1:n.-238-23223G>A
ENST00000560636.5:c.-322-23223G>A	ENSP00000453420.1:n.-322-23223G>A
XM_011522075.1:c.-238-23223G>A	XP_011520377.1:n.-238-23223G>A
XM_011522075.2:c.-238-23223G>A	XP_011520377.1:n.-238-23223G>A
XM_017022617.2:c.-238-23223G>A	XP_016878106.1:n.-238-23223G>A
XM_017022620.1:c.-238-23223G>A	XP_016878109.1:n.-238-23223G>A
XM_017022621.1:c.-238-23223G>A	XP_016878110.1:n.-238-23223G>A
XM_024450073.1:c.-238-23223G>A	XP_024305841.1:n.-238-23223G>A
XM_024450074.1:c.-206-23223G>A	XP_024305842.1:n.-206-23223G>A
XM_024450076.1:c.-158-81304G>A	XP_024305844.1:n.-158-81304G>A