Canonical Allele Identifier: CA368025432

Gene: SEMA3D

Linked Data

• MyVariant Identifiers: chr7:g.84651849G>C (hg19) ; chr7:g.85022533G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.85022533G>C , CM000669.2:g.85022533G>C	GRCh38
NC_000007.13:g.84651849G>C , CM000669.1:g.84651849G>C	GRCh37
NC_000007.12:g.84489785G>C	NCBI36
NG_051329.1:g.169323C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284136.11:c.1272C>G MANE Select	ENSP00000284136.6:p.His424Gln
ENST00000284136.10:c.1272C>G	ENSP00000284136.6:p.His424Gln
ENST00000484038.1:n.398C>G
NM_152754.2:c.1272C>G	NP_689967.2:p.His424Gln
XM_011515960.1:c.1272C>G	XP_011514262.1:p.His424Gln
XM_011515961.1:c.690C>G	XP_011514263.1:p.His230Gln
XM_011515962.1:c.189C>G	XP_011514264.1:p.His63Gln
XM_011515961.2:c.690C>G	XP_011514263.1:p.His230Gln
XM_017011873.1:c.1272C>G	XP_016867362.1:p.His424Gln
NM_001384900.1:c.1272C>G MANE Select	NP_001371829.1:p.His424Gln
NM_001384901.1:c.1272C>G	NP_001371830.1:p.His424Gln
NM_001384902.1:c.1272C>G	NP_001371831.1:p.His424Gln
NM_001384903.1:c.1272C>G	NP_001371832.1:p.His424Gln
NM_152754.3:c.1272C>G	NP_689967.2:p.His424Gln