Canonical Allele Identifier: CA14170074

Gene: SEMA6D

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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