Canonical Allele Identifier: CA321011541
Gene: DSCAM HGNC NCBI
DSCAM-IT1 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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