Canonical Allele Identifier: CA15989065
Gene: DSCAM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.40803034A>G , CM000683.2:g.40803034A>G GRCh38
NC_000021.8:g.42174960A>G , CM000683.1:g.42174960A>G GRCh37
NC_000021.7:g.41096830A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000400454.6:c.43+43585T>C MANE Select ENSP00000383303.1:n.43+43585T>C
ENST00000400454.5:c.43+43585T>C ENSP00000383303.1:n.43+43585T>C
NM_001271534.1:c.43+43585T>C NP_001258463.1:n.43+43585T>C
NM_001389.3:c.43+43585T>C NP_001380.2:n.43+43585T>C
NR_073202.1:n.495+43585T>C
XM_011529480.1:c.55+43573T>C XP_011527782.1:n.55+43573T>C
NM_001271534.2:c.43+43585T>C NP_001258463.1:n.43+43585T>C
NM_001389.4:c.43+43585T>C NP_001380.2:n.43+43585T>C
NR_073202.2:n.521+43585T>C
NM_001389.5:c.43+43585T>C MANE Select NP_001380.2:n.43+43585T>C
NM_001271534.3:c.43+43585T>C NP_001258463.1:n.43+43585T>C
NR_073202.3:n.540+43585T>C
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