Canonical Allele Identifier: CA2389936569
Gene: DSCAM HGNC NCBI
DSCAM-IT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.40621781T>A , CM000683.2:g.40621781T>A GRCh38
NC_000021.8:g.41993707T>A , CM000683.1:g.41993707T>A GRCh37
NC_000021.7:g.40915577T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000400454.6:c.508+71029A>T (DSCAM) MANE Select ENSP00000383303.1:n.508+71029A>T
ENST00000400454.5:c.508+71029A>T (DSCAM) ENSP00000383303.1:n.508+71029A>T
NM_001271534.1:c.508+71029A>T (DSCAM) NP_001258463.1:n.508+71029A>T
NM_001389.3:c.508+71029A>T (DSCAM) NP_001380.2:n.508+71029A>T
NR_046774.2:n.213-381A>T (DSCAM-IT1)
NR_073202.1:n.960+71029A>T (DSCAM)
XM_011529480.1:c.520+71029A>T (DSCAM) XP_011527782.1:n.520+71029A>T
NM_001271534.2:c.508+71029A>T (DSCAM) NP_001258463.1:n.508+71029A>T
NM_001389.4:c.508+71029A>T (DSCAM) NP_001380.2:n.508+71029A>T
NR_073202.2:n.986+71029A>T (DSCAM)
NM_001389.5:c.508+71029A>T (DSCAM) MANE Select NP_001380.2:n.508+71029A>T
NM_001271534.3:c.508+71029A>T (DSCAM) NP_001258463.1:n.508+71029A>T
NR_073202.3:n.1005+71029A>T (DSCAM)
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