Canonical Allele Identifier: CA10031751

Gene: DSCAM

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.40692859C>T , CM000683.2:g.40692859C>T	GRCh38
NC_000021.8:g.42064785C>T , CM000683.1:g.42064785C>T	GRCh37
NC_000021.7:g.40986655C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001389.5:c.459G>A MANE Select	NP_001380.2:p.Ala153=
ENST00000400454.6:c.459G>A MANE Select	ENSP00000383303.1:p.Ala153=
NM_001271534.1:c.459G>A	NP_001258463.1:p.Ala153=
NM_001271534.2:c.459G>A	NP_001258463.1:p.Ala153=
NM_001271534.3:c.459G>A	NP_001258463.1:p.Ala153=
NM_001389.3:c.459G>A	NP_001380.2:p.Ala153=
NM_001389.4:c.459G>A	NP_001380.2:p.Ala153=
NR_073202.1:n.911G>A
NR_073202.2:n.937G>A
NR_073202.3:n.956G>A
ENST00000400454.5:c.459G>A	ENSP00000383303.1:p.Ala153=
XM_011529480.1:c.471G>A	XP_011527782.1:p.Ala157=