Canonical Allele Identifier: CA161799440

Gene: SEMA3A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.84281955G>A , CM000669.2:g.84281955G>A	GRCh38
NC_000007.13:g.83911271G>A , CM000669.1:g.83911271G>A	GRCh37
NC_000007.12:g.83749207G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424555.5:c.-83+25252C>T	ENSP00000404800.1:n.-83+25252C>T
ENST00000448879.5:c.-83+25252C>T	ENSP00000402093.1:n.-83+25252C>T
XM_005250110.2:c.-83+25252C>T	XP_005250167.1:n.-83+25252C>T
XM_005250111.3:c.-83+25252C>T	XP_005250168.1:n.-83+25252C>T
XM_011515734.1:c.-83+13087C>T	XP_011514036.1:n.-83+13087C>T
XM_005250110.3:c.-83+25252C>T	XP_005250167.1:n.-83+25252C>T
XM_005250111.4:c.-83+25252C>T	XP_005250168.1:n.-83+25252C>T
XM_011515734.3:c.-83+13087C>T	XP_011514036.1:n.-83+13087C>T
XM_024446633.1:c.-83+25252C>T	XP_024302401.1:n.-83+25252C>T