Canonical Allele Identifier: CA843158009
Gene: SEMA3D HGNC NCBI

Linked Data

dbSNP Id: rs1337253488

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.85084449_85084451del , CM000669.2:g.85084449_85084451del GRCh38
NC_000007.13:g.84713765_84713767del , CM000669.1:g.84713765_84713767del GRCh37
NC_000007.12:g.84551701_84551703del NCBI36
NG_051329.1:g.107407_107409del

Transcript Alleles

HGVS Amino-acid change
ENST00000284136.11:c.313-2870_313-2868del MANE Select ENSP00000284136.6:n.313-2870_313-2868del
ENST00000284136.10:c.313-2870_313-2868del ENSP00000284136.6:n.313-2870_313-2868del
ENST00000444867.1:c.313-2870_313-2868del ENSP00000401366.1:n.313-2870_313-2868del
NM_152754.2:c.313-2870_313-2868del NP_689967.2:n.313-2870_313-2868del
XM_011515960.1:c.313-2870_313-2868del XP_011514262.1:n.313-2870_313-2868del
XM_011515961.1:c.-270-2870_-270-2868del XP_011514263.1:n.-270-2870_-270-2868del
XM_011515961.2:c.-270-2870_-270-2868del XP_011514263.1:n.-270-2870_-270-2868del
XM_017011873.1:c.313-2870_313-2868del XP_016867362.1:n.313-2870_313-2868del
NM_001384900.1:c.313-2870_313-2868del MANE Select NP_001371829.1:n.313-2870_313-2868del
NM_001384901.1:c.313-2870_313-2868del NP_001371830.1:n.313-2870_313-2868del
NM_001384902.1:c.313-2870_313-2868del NP_001371831.1:n.313-2870_313-2868del
NM_001384903.1:c.313-2870_313-2868del NP_001371832.1:n.313-2870_313-2868del
NM_152754.3:c.313-2870_313-2868del NP_689967.2:n.313-2870_313-2868del