Canonical Allele Identifier: CA4488827

Gene: PLXNA4

Linked Data

• ClinVar Variation Id: 3036086
• ClinVar RCV Id: RCV003904452
• dbSNP Id: rs199878062
• ExAC: 7:131815233 G / A
• gnomAD v2: 7-131815233-G-A
• gnomAD v3: 7-132130474-G-A
• gnomAD v4: 7-132130474-G-A
• MyVariant Identifiers: chr7:g.131815233G>A (hg19) ; chr7:g.132130474G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.132130474G>A , CM000669.2:g.132130474G>A	GRCh38
NC_000007.13:g.131815233G>A , CM000669.1:g.131815233G>A	GRCh37
NC_000007.12:g.131465773G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321063.9:c.*5C>T MANE Select	ENSP00000323194.4:n.*5C>T
ENST00000321063.8:c.*5C>T	ENSP00000323194.4:n.*5C>T
ENST00000359827.7:c.*5C>T	ENSP00000352882.3:n.*5C>T
NM_020911.1:c.*5C>T	NP_065962.1:n.*5C>T
XM_005250686.3:c.*5C>T	XP_005250743.1:n.*5C>T
XM_006716171.2:c.*5C>T	XP_006716234.1:n.*5C>T
XM_005250686.5:c.*5C>T	XP_005250743.1:n.*5C>T
XM_006716171.4:c.*5C>T	XP_006716234.1:n.*5C>T
XM_017012779.1:c.*5C>T	XP_016868268.1:n.*5C>T
NM_001393897.1:c.*5C>T	NP_001380826.1:n.*5C>T
NM_020911.2:c.*5C>T MANE Select	NP_065962.1:n.*5C>T