Canonical Allele Identifier: CA2838655965

Gene: WNT7A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13854808G>T , CM000665.2:g.13854808G>T	GRCh38
NC_000003.11:g.13896305G>T , CM000665.1:g.13896305G>T	GRCh37
NC_000003.10:g.13871306G>T	NCBI36
NG_008088.1:g.30314C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285018.5:c.299-5C>A MANE Select	ENSP00000285018.4:n.299-5C>A
ENST00000285018.4:c.299-5C>A	ENSP00000285018.4:n.299-5C>A
NM_004625.3:c.299-5C>A	NP_004616.2:n.299-5C>A
XM_011534090.1:c.98-5C>A	XP_011532392.1:n.98-5C>A
XM_011534091.1:c.98-5C>A	XP_011532393.1:n.98-5C>A
XM_011534091.2:c.98-5C>A	XP_011532393.1:n.98-5C>A
NM_004625.4:c.299-5C>A MANE Select	NP_004616.2:n.299-5C>A