Canonical Allele Identifier: CA2175117165
Gene: SEMA6D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.47600101G>C , CM000677.2:g.47600101G>C GRCh38
NC_000015.9:g.47892298G>C , CM000677.1:g.47892298G>C GRCh37
NC_000015.8:g.45679590G>C NCBI36
NG_029119.1:g.420896G>C
NG_029119.2:g.420896G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000537942.5:c.-86-764G>C ENSP00000442040.1:n.-86-764G>C
ENST00000558014.5:c.-86-764G>C ENSP00000452815.1:n.-86-764G>C
ENST00000559184.5:c.-86-764G>C ENSP00000453097.1:n.-86-764G>C
ENST00000560636.5:c.-170-764G>C ENSP00000453420.1:n.-170-764G>C
NM_001198999.1:c.-86-764G>C NP_001185928.1:n.-86-764G>C
XM_011522075.1:c.-86-764G>C XP_011520377.1:n.-86-764G>C
XR_932195.1:n.2385C>G
XR_932196.1:n.1973C>G
XR_932197.1:n.1645C>G
XM_011522075.2:c.-86-764G>C XP_011520377.1:n.-86-764G>C
XM_017022617.2:c.-86-764G>C XP_016878106.1:n.-86-764G>C
XM_017022620.1:c.-86-764G>C XP_016878109.1:n.-86-764G>C
XM_017022621.1:c.-86-764G>C XP_016878110.1:n.-86-764G>C
XM_024450073.1:c.-86-764G>C XP_024305841.1:n.-86-764G>C
XM_024450074.1:c.-55+129556G>C XP_024305842.1:n.-55+129556G>C
XM_024450076.1:c.-86-764G>C XP_024305844.1:n.-86-764G>C
XR_001751512.1:n.8329C>G
XR_001751513.1:n.7424C>G
XR_001751514.1:n.7379C>G
XR_001751515.1:n.7917C>G
NM_001198999.2:c.-86-764G>C NP_001185928.1:n.-86-764G>C