Canonical Allele Identifier: CA2838208147
Gene: DSCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.40708872T>A , CM000683.2:g.40708872T>A GRCh38
NC_000021.8:g.42080798T>A , CM000683.1:g.42080798T>A GRCh37
NC_000021.7:g.41002668T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000400454.6:c.44-101A>T MANE Select ENSP00000383303.1:n.44-101A>T
ENST00000400454.5:c.44-101A>T ENSP00000383303.1:n.44-101A>T
NM_001271534.1:c.44-101A>T NP_001258463.1:n.44-101A>T
NM_001389.3:c.44-101A>T NP_001380.2:n.44-101A>T
NR_073202.1:n.496-101A>T
XM_011529480.1:c.56-101A>T XP_011527782.1:n.56-101A>T
NM_001271534.2:c.44-101A>T NP_001258463.1:n.44-101A>T
NM_001389.4:c.44-101A>T NP_001380.2:n.44-101A>T
NR_073202.2:n.522-101A>T
NM_001389.5:c.44-101A>T MANE Select NP_001380.2:n.44-101A>T
NM_001271534.3:c.44-101A>T NP_001258463.1:n.44-101A>T
NR_073202.3:n.541-101A>T